Safety Recalls

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15,200 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 4,201–4,250 of 15,200

Food Recall · September 26, 2025
Wegmans Food Markets, Inc.
Wegmans Large Ultimate Plain Cheesecake, Net Wt. 50 oz. (3.13lb) (1.42kg)
Contains undeclared pecans
Class I
Food Recall · September 26, 2025
WHOLESALE PRODUCE SUPPLY LLC DBA
Cut Fresh Fruit Salad. 6/6 oz. Harvest Cuts. Contains: Cantaloupe, Honeydew, Red Grape, Strawberry. Keep Refrigerated. Packed in the following container sizes: 1. 6/6 oz. UPC 7 90629-1182
Potential Listeria monocytogenes contamination.
Class I
Food Recall · September 26, 2025
WHOLESALE PRODUCE SUPPLY LLC DBA
Cut Fresh Cantaloupe Chunks packaged into the following size containers some under brand names Fresh & Finest or Harvest Cuts: 1. CANTALOUPE CHUNKS "PRMK" 30/2 OZ 2. CANTALOUPE CHUNKS "HC" 6/6
Potential Listeria monocytogenes contamination.
Class I
Medical Device Recall · September 26, 2025
DSAART LLC
Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/Catalog Number: 500-106-5 Pectoral Implant style 1 size 6 left UDI-DI code: B4905001065 500-106-6 Pectoral Implant style 1
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Prepared with Balanced Heparin Model 06 0186 Product Description: A clear, plastic capillary blood collection tube coated with Heparin
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Food Recall · September 26, 2025
Albertsons Companies LLC
Grilled Chicken & Basil Pasta Extra Large UPC 213035 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Class I
Medical Device Recall · September 26, 2025
Integra LifeSciences Corp. (NeuroSciences)
CODMAN Disposable Perforator 11mm. Cranial Perforator.
Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution.
Class I
Food Recall · September 26, 2025
MAYEJ COMERCIALIZADORA S. de R.L. de C.V.
Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.
pathogen Cyclospora cayetanensis
Class II
Food Recall · September 26, 2025
Albertsons Companies LLC
Smoked Mozzarella Penne Salad Kit, UPC 271876 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne pasta ingredient which was recalled due to Listeria monocytogenes.
Class I
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL End Caps for SAFE-T-FILL Blood Gas Capillaries; Fits outer diameter 1.6 - 2.1mm, Model 06 0402 Product Description: A clear, plastic capillary blood collection tube
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator and Serum Separator Gel; Red Model/Catalog Number: 07 7120 Product Description: The SAFE-T-FILL Capillary Blood
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L; Untreated, Blue Markings Model/Catalog Number: 06 0508 Product Description: A clear, plastic capillary blood collection tube
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Food Recall · September 26, 2025
Albertsons Companies LLC
Ready Meals Basil Pesto Bowtie Pasta Salad, UPC 291308 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, an
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Class I
Food Recall · September 26, 2025
WHOLESALE PRODUCE SUPPLY LLC DBA
Cut Fresh Melon Mix. Contains: Cantaloupe, Honeydew, Watermelon. Keep Refrigerated. Packed under the following brands and sizes: 1. Melon Mix "HC" 4/16 oz. Harvest Cuts UPC 7 90629-11844 5.
Potential Listeria monocytogenes contamination.
Class I
Medical Device Recall · September 26, 2025
GE Healthcare Finland Oy
B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160000-103 6160000-104 6160000-105 6160001-063 6160001-064 6160
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
Class II
Food Recall · September 26, 2025
Reser's Fine Foods, Inc.
Fresh Creative Foods (FCF) item #404284 Smoked Mozzarella Penne Salad Kit, UPC #13454 37904. Perishable/Refrigerated product. Net wt. 13lbs. This kit contains 2/3lbs. sealed bag of affected Penne Past
Salad Kits are recalled due to potential contamination with Listeria monocytogenes.
Class I
Medical Device Recall · September 26, 2025
GE Healthcare Finland Oy
CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
Class II
Food Recall · September 26, 2025
The Kroger Co
Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at deli service counters) or UPC 217573-2XXXX (sold as Grab-n-Go packages in deli depar
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
Class I
Food Recall · September 26, 2025
WHOLESALE PRODUCE SUPPLY LLC DBA
Cut Fresh Luau Blend Fruit Mix "F&F". 4/10 oz. Fresh & Finest. Contains: Cantaloupe, Honeydew, Pineapple, Red Grapes, Strawberry, Blueberry. Keep Refrigerated. UPC 0 70253-00572 5. Packed
Potential Listeria monocytogenes contamination.
Class I
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0009 Product Description: A clear, plastic capillary blood collection tube
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Food Recall · September 26, 2025
SLR Food Distribution, Inc.
Wise Wife Ground Cinnamon
Contains elevated levels of lead
Class II
Food Recall · September 26, 2025
Wegmans Food Markets, Inc.
Large Ultimate Fresh Fruit Topped Cheesecake, Net Wt. 55 oz. (3.44 lb) (1.56kg)
Contains undeclared pecans
Class I
Food Recall · September 26, 2025
WHOLESALE PRODUCE SUPPLY LLC DBA
Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, Watermelon and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix CHWG (MCT) 1/5 lb. UPC 7 90629-1117
Potential Listeria monocytogenes contamination.
Class I
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L; Prepared with Balanced Heparin, Model/Catalog Number: 06 0187 Product Description: A clear, plastic capillary blood collection tube
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Sodium Fluoride; Gray Model/Catalog Number: 07 7340 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Medical Device Recall · September 26, 2025
DSAART LLC
Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Implant style 1 size 3 UDI-DI code: B490502103 502-104 - Calf Implant style 1 size 4 UDI-DI code:
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
Class II
Medical Device Recall · September 26, 2025
Zimmer, Inc.
Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing, Model/Catalog Number: 110031012; semi constrained hip prosthesis
Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E¿ Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, however, the implant inside the package is a Size G 46 mm, and vice versa.
Class II
Medical Device Recall · September 26, 2025
DSAART LLC
Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Number: 401-202-5 Malar Implant style 2 size 2 left UDI-DI code: B4904012025 401-202-6 Malar Implant style 2 size 2 righ
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0007 Product Description: A clear, plastic capillary blood collection tube
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07 7251 Product Description: The SAFE-T-FILL Capillary Blood Collection System is
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Medical Device Recall · September 26, 2025
GE Healthcare Finland Oy
Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
Class II
Medical Device Recall · September 26, 2025
Synthes (USA) Products LLC
LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 46MM / XL25/ STER. Product Code: 04.045.346TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
Although the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged and labeled as 46mm, while 46mm screws were packaged and labeled as 42mm.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L; Plastic, Ammonium Heparinized, Red Marking Model/Catalog Number: 06 0507 Product Description: A clear, plastic capillary blood collection tube c
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Medical Device Recall · September 26, 2025
Zimmer, Inc.
Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 46 mm O.D., Size G, Bearing, Model/Catalog Number: 110031013; semi constrained hip prosthesis
Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E¿ Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, however, the implant inside the package is a Size G 46 mm, and vice versa.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator; Amber Microtube, Red Model/Catalog Number: 07 7450 Product Description: The SAFE-T-FILL Capillary Blood Collect
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Medical Device Recall · September 26, 2025
GE Healthcare Finland Oy
BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, revision S
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
Class II
Medical Device Recall · September 26, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 115 ¿L; Prepared with Balanced Heparin Model/Catalog Number: 06 0185 Product Description: A clear, plastic capillary blood collection tube
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II
Food Recall · September 25, 2025
Nate's Fine Foods, LLC
TAYLOR FARMS COOKED ROTINI MAP 8 X 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED
Potential contamination with Listeria monocytogenes.
Class I
Consumer Product Recall · September 25, 2025
Sunbeam Products Inc., of Atlanta, Georgia
Oster French Door Countertop Ovens
The oven's doors can unexpectedly close, posing a burn hazard to consumers.
Unclassified
Food Recall · September 25, 2025
Nate's Fine Foods, LLC
COOKED LINGUINE PASTA 5LB POUCHES PERISHABLE KEEP REFRIGERATED
Potential contamination with Listeria monocytogenes.
Class I
Food Recall · September 25, 2025
Nate's Fine Foods, LLC
COOKED LINGUINE PASTA 6 x 5 lb Net Wt. 30lbs (13.60kg) PERISHABLE KEEP FROZEN
Potential contamination with Listeria monocytogenes.
Class I
Food Recall · September 25, 2025
Nate's Fine Foods, LLC
TAYLOR FARMS COOKED FARFALLE MAP 8 X 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED
Potential contamination with Listeria monocytogenes.
Class I
Food Recall · September 25, 2025
Nate's Fine Foods, LLC
FRESH CREATIVE FOODS COOKED FARFALLE PASTA 8 x 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED
Potential contamination with Listeria monocytogenes.
Class I
Medical Device Recall · September 25, 2025
PHILIPS MEDICAL SYSTEMS
Model: Incisive CT; Product Code (REF): (1) 728143, (2) 728144; Software Versions: 5.1.0.X & 5.1.1.X;
Issue 1: The potential for unintentional continued gantry/couch movement when a specific button series is used requiring use of manual stop. Issue 2. When performing a helical/Axial scan with ORI (Dose Right index)/ DOM (Dose Modulation), the WED (Water Equivalent Diameter) value might set itself to zero, and this may lead to an insufficient dose setting after the surview. If operator misses the insufficient dose and the WED value in User Interface and continues with the subsequent helical/Axial scans, then the obtained images will be noisy due to low dose setting. Issue 3: Due to a software failure, the ECG wave file is not saved. As a result, the cardiac offline image reconstruction fails due to the missing ECG wave file, and the user might rescan the patient. Issue 4: This issue is software fault in which the patient orientation will be changed to NULL under specific random scenarios resulting in radiation being delivered from the wrong orientation (surview scan) or in the wrong position (clinical scan) and will generate incorrect and undiagnosable surview/clinical images. Patients may be rescanned for surview and/or clinical images. Issue 5: During scanning, the preview image display is not consistent, the images are not arriving at a fixed rate, skipping images from time to time during scanning. The obtained images might not support making the clinical diagnosis and the user might decide to re-scan the patient. Issue 6: If a user presses the left and middle/right mouse buttons together or afterwards in a short time, both commands are executed and an incorrect auto ROI is created. This ROI coordinates won t be assigned as the object is empty. As a result, the threshold of contrast level will not be reached in the UI and this will prevent the system from automatically triggering the subsequent clinical scan. There is potential safety risk identified for additionally tracker shots and/or rescan of a patient when the clinical scan is not triggered. This issue only affects the manual ROI process.
Class II
Medical Device Recall · September 25, 2025
LeMaitre Vascular, Inc.
Artegraft¿ Collagen Vascular Graft; REF: AG1015;
The device was incorrectly packed in the wrong size labeled outer packaging.
Class II
Consumer Product Recall · September 25, 2025
Mad Rabbit Inc., of Los Angeles, California
RELIEVE Numbing Cream
The numbing cream contains lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The numbing cream's packaging is not child-resistant, posing a risk of serious injury or death from poisoning, if the contents are swallowed by young children.
Unclassified
Consumer Product Recall · September 25, 2025
Zhejiang Xidamen New Material Co. Ltd., of China, doing business as Amazon seller Persilu
Persilux Zebra Blinds
The recalled blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The blinds violate the federal rule for window coverings and present a substantial product hazard. In addition, the blinds also violate labeling requirements for window coverings.
Unclassified
Drug Recall · September 25, 2025
SV Labs Prescott Corporation
Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per tube, Mfd. for: ALOE UP, 9700 W. 76th St., Ste 112, Eden Prairie, Minnesota 55344
cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing.
Class II
Food Recall · September 25, 2025
Georgia Nut Co
tru fru Dark + White Chocolate Freeze-Dried Strawberries. 1.7oz retail pouch UPC 850048358331. 12 retail units per case. 3.4oz retail pouch UPC 850048358270. 6 retail units per case. 13oz retail pou
potential for metal in product
Class II
Medical Device Recall · September 25, 2025
PHILIPS MEDICAL SYSTEMS
Model: Incisive CT for Brazil SKD; Product Code (REF): 728146; Software Versions: 5.1.0.X & 5.1.1.X;
Issue 1: The potential for unintentional continued gantry/couch movement when a specific button series is used requiring use of manual stop. Issue 2. When performing a helical/Axial scan with ORI (Dose Right index)/ DOM (Dose Modulation), the WED (Water Equivalent Diameter) value might set itself to zero, and this may lead to an insufficient dose setting after the surview. If operator misses the insufficient dose and the WED value in User Interface and continues with the subsequent helical/Axial scans, then the obtained images will be noisy due to low dose setting. Issue 3: Due to a software failure, the ECG wave file is not saved. As a result, the cardiac offline image reconstruction fails due to the missing ECG wave file, and the user might rescan the patient. Issue 4: This issue is software fault in which the patient orientation will be changed to NULL under specific random scenarios resulting in radiation being delivered from the wrong orientation (surview scan) or in the wrong position (clinical scan) and will generate incorrect and undiagnosable surview/clinical images. Patients may be rescanned for surview and/or clinical images. Issue 5: During scanning, the preview image display is not consistent, the images are not arriving at a fixed rate, skipping images from time to time during scanning. The obtained images might not support making the clinical diagnosis and the user might decide to re-scan the patient. Issue 6: If a user presses the left and middle/right mouse buttons together or afterwards in a short time, both commands are executed and an incorrect auto ROI is created. This ROI coordinates won t be assigned as the object is empty. As a result, the threshold of contrast level will not be reached in the UI and this will prevent the system from automatically triggering the subsequent clinical scan. There is potential safety risk identified for additionally tracker shots and/or rescan of a patient when the clinical scan is not triggered. This issue only affects the manual ROI process.
Class II