Safety Recalls

17,567 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 5,751–5,800 of 17,567

• Medical Device Recall · September 30, 2025

  Medline Industries, LP

  MEDLINE convenience kits labeled as: GP-LEEP PACK-LF, REF PHS396969004F

  Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.

  Class II

• Food Recall · September 29, 2025

  Eli's Cheesecake Company

  Wegmans Ultimate Plain Cheesecake Large Net Wt 3.13 lb (1.42kg), shrink wrapped in a collar, 8 cakes per wholesale case

  undeclared pecan

  Class I

• Drug Recall · September 29, 2025

  Acella Pharmaceuticals, LLC

  Doxycycline Hyclate Tablets, USP 100 mg*, 500-count bottle, Rx Only, Distributed by: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, NDC 42192-501-05.

  Failed dissolution specifications: Stability testing found that the lot did not meet dissolution specifications.

  Class II

• Drug Recall · September 29, 2025

  Medline Industries, LP

  Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Driv

  Subpotent Drug

  Class II

• Drug Recall · September 29, 2025

  Acuity Specialty Products, Inc.

  AFCO, Hand Sanitizer (Isopropyl Alcohol-Based, Product 5515), Manufactured by: AFCO, 550 Development Avenue, Chambersburg, PA 17201, Toll Free: 800-345-1329, Package Configuration: a) 4x1 Gallon Case,

  cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.

  Class II

• Food Recall · September 29, 2025

  EGGS UNLIMITED LLC

  Big Y Brown Jumbo A 12ct Eggs; UPC: 018894319146 Simple Truth Cage Free Brown Large AA 12ct; UPC: 011110797698 Stater Bros Cage Free Large AA 18ct; 074175001650 That's Smart Cage Free Large AA 60ct; 1

  Firm received, repackaged eggs that are potentially contamination with Salmonella.

  Class I

• Drug Recall · September 29, 2025

  Acuity Specialty Products, Inc.

  Wyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based, Product 5511), Ethyl Alcohol 60.1%, Manufacture By: AFCO, 550 Development Avenue, Chambersburg, PA 17210, Toll Free: 800-345-1329, Package Config

  cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.

  Class II

• Food Recall · September 29, 2025

  New Age International, Inc.

  Signature brand Enoki Mushroom; 200g; clear plastic package

  Product may be contaminated with Listeria monocytogenes.

  Class I

• Medical Device Recall · September 29, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system

  Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.

  Class II

• Food Recall · September 27, 2025

  Vicky IT Inc.

  Bona Fish

  Fish is un-eviscerated (may be contaminated with Clostridia botulinum), is contaminated with mold, and contains filth (insect larvae)

  Class I

• Food Recall · September 27, 2025

  FreshRealm, Inc

  Marketside Cheesy Cauliflower Au Gratin 12 oz.; UPC: 10194346375445

  Potential contamination with listeria monocytogenes

  Class II

• Food Recall · September 26, 2025

  Reser's Fine Foods, Inc.

  Fresh Creative Foods (FCF) item #404637 Basil Pesto Bowtie Pasta Kit Item V, UPC#13454 38053. Perishable/Refrigerated product. Net wt. 10.5625lbs. This kit contains 2/3lbs. sealed bags of affected Bow

  Salad Kits are recalled due to potential contamination with Listeria monocytogenes.

  Class I

• Food Recall · September 26, 2025

  Albertsons Companies LLC

  READY MEALS Pesto Bowtie Pasta Salad, UPC 27133 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Albertsons, Pavilions, Randalls

  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

  ASP Global, LLC. dba Anatomy Supply Partners, LLC.

  SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Lithium Heparin and Plasma Separator Gel; Green Model/Catalog Number: 07 7221 Product Description: The SAFE-T-FILL Capillary Bl

  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 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 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

• 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

  Wegmans Food Markets, Inc.

  Wegmans Large Ultimate Plain Cheesecake, Net Wt. 50 oz. (3.13lb) (1.42kg)

  Contains undeclared pecans

  Class I

• Medical Device Recall · September 26, 2025

  ASP Global, LLC. dba Anatomy Supply Partners, LLC.

  Mixing Fleas for SAFE-T-FILL Blood Gas Capillaries, Model 07 9503

  Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

  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

• 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 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 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 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

• Food Recall · September 26, 2025

  WHOLESALE PRODUCE SUPPLY LLC DBA

  Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, Pineapple, and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix CHPG (MCT) 1/5 lb. 2. Fruit Medle

  Potential Listeria monocytogenes contamination.

  Class I

• 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

• 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

  Ready Meals Smoked Mozzarella With Hot Links Extra Large, UPC 200003 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safew

  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

  Integra LifeSciences Corp. (NeuroSciences)

  CODMAN Disposable Perforator 9mm. 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

• 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

• Medical Device Recall · September 26, 2025

  ASP Global, LLC. dba Anatomy Supply Partners, LLC.

  SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Untreated. Model 06 0199 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

  Synthes (USA) Products LLC

  LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 42MM / XL25/ STER. Product Code: 04.045.342TS. 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

  DSAART LLC

  Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Numbers: 600-601 - Silicone Carving Implant Style 6 Size 1 UDI-DI code: B490600601 600-602 - Silicone Ca

  Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

  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

• 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 Clot Activator; Red Model/Catalog Number: 07 7151 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a c

  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.

  AFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Lithium Heparin and Plasma Separator Gel; Green Model/Catalog Number: 07 7220 Product Description: The SAFE-T-FILL Capillary Blo

  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 Lithium Heparin; Green Model/Catalog Number: 07 7250 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

  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

• Medical Device Recall · September 26, 2025

  ASP Global, LLC. dba Anatomy Supply Partners, LLC.

  SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07 6101 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

• Food Recall · September 26, 2025

  Albertsons Companies LLC

  Basil Pesto Bowtie Pasta Salad, UPC 294921 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Albertsons, Pavilions, Randalls, Safew

  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

  ASP Global, LLC. dba Anatomy Supply Partners, LLC.

  SAFE-T-FILL Magnetic Rings for SAFE-T-FILL Blood Gas Capillaries, Model 07 9502

  Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

  Class II

• Food Recall · September 26, 2025

  Reser's Fine Foods, Inc.

  Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated product. Net wt. 10.3125lbs. This kit contains 2/3lb. sealed bags of affected Bowtie Pas

  Salad Kits are recalled due to potential contamination with Listeria monocytogenes.

  Class I

• 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 26, 2025

  SLR Food Distribution, Inc.

  Wise Wife Ground Cinnamon

  Contains elevated levels of lead

  Class II

• Food Recall · September 26, 2025

  WHOLESALE PRODUCE SUPPLY LLC DBA

  Cut Fresh Fruit Tray with Strawberries. 2.5 LB Harvest Cuts. Keep Refrigerated. UPC 7 90629-08132 9. Packed by WPS, Minneapolois, MN

  Potential Listeria monocytogenes contamination.

  Class I

• Food Recall · September 26, 2025

  Wegmans Food Markets, Inc.

  Wegmans Large Ultimate Blueberry Topped Cheesecake, Net Wt. 58 oz (3.63 lb) (1.64 kg)

  Contains undeclared pecans

  Class I

• Food Recall · September 26, 2025

  Wegmans Food Markets, Inc.

  Wegmans Large Ultimate Cherry Topped Cheesecake, Net Wt. 58 oz. (3.63 lb) (1.64kg)

  Contains undeclared pecans

  Class I

• Medical Device Recall · September 26, 2025

  DSAART LLC

  Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog Numbers: 400-0101 Chin Implant style 1 size 1 UDI-DI code: B490400101 400-0103 Chin Implant style 1 size 3 UDI-DI code: B

  Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

  Class II