Safety Recalls

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15,259 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 5,201–5,250 of 15,259

Food Recall · August 5, 2025
Kobayashi Noodle U.S.A.
Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (16049) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens: Wheat, Egg
Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.
Class II
Drug Recall · August 5, 2025
Cardinal Health Inc.
Enoxaparin Sodium Injection, USP, 30 mg/0.3 mL, packaged in 0.3 mL prefilled syringes further packaged in bags of 5 prefilled syringes, Rx Only, Dist. by: Sandoz Inc., Princeton, NJ 08540, Outer packa
Correct Labeled Product Mispack: Bags labeled for Enoxaparin Sodium Injection, 80 mg/0.8 mL, contained Enoxaparin Sodium Injection, 30 mg/0.3 mL
Class II
Food Recall · August 5, 2025
Khee Trading, Inc.
Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads: HAFL SHELL OYSTER Spec: 144PCS; Imported by: Khee Trading Inc., Compton, CA Side
Imported Frozen Oyster potentially contaminated with Norovirus.
Class II
Medical Device Recall · August 5, 2025
Integra LifeSciences Corp. (NeuroSciences)
Brand Name: MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet Dressing Model/Catalog Number: 31720, 31740 Product Description: MEDIHONEY¿ Adhesive Hydrogel Sheet Dressing with Leptosperm
Packaging failures were identified which could lead to a breach in the sterile barrier.
Class II
Medical Device Recall · August 4, 2025
WASATCH PHOTONICS
Wasatch Photonics 785/830-SR and 785-ER-ILC Raman Spectrometers, Product Models: 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC,785-ER-ILC.
Two new potential laser safety failure modes have been identified in the product design. Overcurrent of laser diode, and a fail-unsafe mode. The failure modes have never been found to occur in these models, whether in the field or factory, but could potentially occur under excessive force or extreme, continuous vibration.
Class II
Medical Device Recall · August 4, 2025
Baxter Healthcare Corporation
Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).
Class I
Medical Device Recall · August 4, 2025
AVID Medical, Inc.
Halyard, CPT BASIC IR PACK. Model Number: 1646381. Convenience kit.
Potential for open header bag seals, compromising sterility.
Class II
Medical Device Recall · August 4, 2025
Baxter Healthcare Corporation
Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).
Class I
Drug Recall · August 4, 2025
PFIZER INC
Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045, USA. NDC 0409-4933-05. Case: NDC 0409-4933-10.
Lack of Assurance of Sterility.
Class II
Medical Device Recall · August 4, 2025
Merit Medical Systems, Inc.
PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A, K12T-10798A, MAP800/B, MAP800/T, MAP801/B, MAP802/B, MAP802/CNB, MAP802/T, MAP80
Hemostasis valve has a manufacturing defect and when used the valve cap may remain depressed, leading to potential leakage, which may result in procedure inconvenience and/or hemorrhage.
Class II
Medical Device Recall · August 4, 2025
Baxter Healthcare Corporation
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).
Class I
Drug Recall · August 4, 2025
B BRAUN MEDICAL INC
0.9% Sodium Chloride Injection USP, L 8000, 1000mL Excel Container, Rx Only, Sterile, nonpyrogenic, single dose container, B. Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7800-00.
Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
Class II
Drug Recall · August 4, 2025
B BRAUN MEDICAL INC
Lactated Ringer's Injection USP, L 7500, 1000mL Excel Container, Rx Only, Sterile, nonpyrogenic, single dose container, B. Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00.
Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
Class II
Drug Recall · August 4, 2025
PFIZER INC
Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-6637-24. Case NDC: 00409-6637-14.
Lack of Assurance of Sterility.
Class II
Food Recall · August 4, 2025
Neuhaus nv
NEUHAUS brand ORIGINAL BELGIAN CHOCOLATE; POPPING MILK CHOCOLATES WITH COOKIES; 4.23 oz - 120g; (EN)Chocolates - INGREDIENTS: milk chocolate (sugar, whole milk powder, cocoa mass, cocoa butter, emulsi
Product contains undeclared wheat.
Class I
Food Recall · August 4, 2025
Hans Kissle Company, LLC
Hans Kissle Red Bliss Potato Salad
Contains undeclared wheat. The top label identifies the product as potato salad, but the unit contains pasta salad.
Class II
Medical Device Recall · August 4, 2025
AVID Medical, Inc.
Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
Potential for open header bag seals, compromising sterility.
Class II
Medical Device Recall · August 4, 2025
Beckman Coulter Inc.
DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without ISE, REF: C6352; part of the DxC 500i Clinical Analyzer
On a clinical analyzer, when ordering a Clinical Chemistry (CC) combination test simultaneously with an Immunoassay (IA) test, if the IA test is processed between the CC tests, CC sample status will remain In Progress with no errors, may cause processing delays.
Class II
Medical Device Recall · August 1, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x, R2.x). Labeled as the following with corresponding model numbers: 1. Azurion 3 M12, Model Number 722063. 2. Azurion
Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.
Class II
Medical Device Recall · August 1, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series. Labeled as the following with corresponding model numbers: 1. Allura Xper FD10, Model Number 722003. 2. Allura Xper FD10/1
Potential that a component (air baffle) may be missing in some Nehalem FlexVision-2 PCs that are part of the Allura Xper series.
Class II
Food Recall · August 1, 2025
PAX Spices & Labs Inc
Product is distributed in bulk brown paper bags.
Foreign object (metal) in granulated onion ingredient.
Class II
Food Recall · August 1, 2025
SRI SRI TATTVA
Sri Sri Tattva, Ojasvita Chocomalt,7oz / 200g, Paper Pouch, 25 packages per case
Product contains undeclared soy lecithin.
Class II
Food Recall · August 1, 2025
DFA Dairy Brands, LLC
Carton Label: "Friendly's Vanilla Bean"; 48 fl. oz. Lid Label: "Friendly's Cookies and Cream" Product in carton is Cookies and Cream.
Product contains undeclared wheat and soy.
Class II
Medical Device Recall · August 1, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x, R2.x). Labeled as the following with corresponding model numbers: 1. Allura Xper FD10, Model Number 722003 2. Allur
Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.
Class II
Medical Device Recall · July 31, 2025
Medline Industries, LP
Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item Numbers 81102RH 81104RH 81107RH 81174RH
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Class I
Food Recall · July 31, 2025
Jayone Foods, Inc.
Frozen Oyster Meat (IQF), Cert No. KR-15-SP; Processor Name: JBR KR-15-SP; Harvest Date: Feb 06, 2025 Shucked Date: Feb 07,2025 Expiration: 02/06/2027 UPC: 8809366955717
Frozen Oyster product is potentially contaminated with Norovirus
Class II
Consumer Product Recall · July 31, 2025
KidKraft Inc., of Dallas, Texas
KidKraft Farm to Table Model Play Kitchen
If young children are climbing on the counter or crawling through the opening at the back of the play kitchen, their clothing can get caught on the plastic or metal hooks meant to hold toy kitchen accessories such as play pots and pans, posing a strangulation hazard.
Unclassified
Consumer Product Recall · July 31, 2025
TTI Consumer Power Tools, Inc., of Anderson, South Carolina
RIDGID 18Volt Brushless 21-Degree Framing Nailers and RIDGID 18Volt Brushless 30-Degree Framing Nailers
The dual action engagement system on the nailers can malfunction and involuntarily discharge a nail by pulling the trigger alone, posing a laceration hazard to consumers. The nailer should require both the work piece contact element (nose-piece) to be depressed and the trigger to be pulled at the same time in order to discharge a nail.
Unclassified
Medical Device Recall · July 31, 2025
Waldemar Link GmbH & Co. KG (Mfg Site)
LinkSymphoKnee System, Tibial Component, Modular, Symmetric, Sz. 5, CoCrMo/TiNbN, cemented, Fixed. REF Number: 880-100/50
Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.
Class II
Medical Device Recall · July 31, 2025
Medline Industries, LP
Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Class I
Medical Device Recall · July 31, 2025
Medline Industries, LP
Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH 401600RH 401603RH 401606RH 401652RH 401653RH 401654RH 401904RH 401905RH 401908RH 401914RH 401915
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Class I
Medical Device Recall · July 31, 2025
Medline Industries, LP
Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Class I
Food Recall · July 31, 2025
Buffalo Rock Company Inc
7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up Tropical Flavored Soda, UPC (on can): 078000037975, UPC (on carton): 078000037982
Product mislabeled - cans are labeled as Zero Sugar, but contain full sugar product
Class II
Consumer Product Recall · July 31, 2025
DanLoren Group, dba Baby Loren, of Tracy, California
Baby Loren Morning Dresses
The recalled children's loungewear violates the flammability standards for children's sleepwear, posing a risk of burn injuries and death to children.
Unclassified
Consumer Product Recall · July 31, 2025
3Z Brands, of Glendale, Arizona
Amazon Basics Premium Foam Eurotop Mattresses
The recalled mattresses violate a mandatory flammability standard for mattresses, posing a fire hazard and risk of serious injury or death to consumers.
Unclassified
Food Recall · July 31, 2025
Jayone Foods, Inc.
Frozen Oyster Meat (IQF), Cert No. KR-15-SP; Processor Name: JBR KR-15-SP; Harvest Date: Feb 06, 2025 Shucked Date: Feb 07,2025 Expiration: 02/06/2027 UPC: 8809366955717
Frozen Oyster product is potentially contaminated with Norovirus
Class II
Medical Device Recall · July 31, 2025
Lumicell, Inc.
Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Model/Catalog Number: 900-00218 Sterile Cover 10-Pack Shipper Box
The potential of the elastic bands included in the kit detaching or fracturing during surgical procedures. As a result, these failures may pose a risk of retained foreign bodies in the surgical cavity and potentially leading to surgical site infections.
Class II
Medical Device Recall · July 31, 2025
Medline Industries, LP
Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological mapping of cardiac structures. Medline Item Numbers BD710DF282CRH BD710DF282RRH BD710FJ282CRH BD710FJ282RRH
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Class I
Consumer Product Recall · July 31, 2025
Leatherman Tool Group Inc., of Portland, Oregon
Leatherman Charge Plus and Charge Plus TTi Multi-Tools
The tip of the knife blade doesn't fully fold into the handle, posing a laceration hazard.
Unclassified
Consumer Product Recall · July 31, 2025
Dorel Home Furnishings Inc. d/b/a Cosco Home and Office Products, of Columbus, Indiana
Cosco 2-Step Kitchen Stepper
The safety bar can detach or break while in use, posing serious fall and injury hazards to consumers.
Unclassified
Consumer Product Recall · July 31, 2025
IKEA Supply AG, of Switzerland
IKEA 365+ VÄRDEFULL garlic presses
Small metal pieces can detach from the garlic press, posing a laceration or ingestion hazard to consumers.
Unclassified
Consumer Product Recall · July 31, 2025
Tegu Holdings Inc., of Naples, Florida
Magnetic Floating Stackers toys
The recalled magnetic floating stackers toys violate the mandatory standard for toy magnets because they contain magnets that can loosen and detach from the toy, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
Unclassified
Drug Recall · July 30, 2025
GenoGenix LLC
Lysine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Lack of Assurance of Sterility
Class II
Drug Recall · July 30, 2025
GenoGenix LLC
Biotin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Lack of Assurance of Sterility
Class II
Drug Recall · July 30, 2025
GenoGenix LLC
Calcium Chloride for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Lack of Assurance of Sterility
Class II
Drug Recall · July 30, 2025
GenoGenix LLC
Vitamin D3 for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Lack of Assurance of Sterility
Class II
Drug Recall · July 30, 2025
GenoGenix LLC
Retatrutide for Injection, 60mg / 10mL vial, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
Lack of Assurance of Sterility
Class II
Drug Recall · July 30, 2025
Cardinal Health Inc.
RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only, Takeda Pharmaceuticals USA, Cambridge, MA 02142, NDC: 00944-2843-01
CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.
Class II
Drug Recall · July 30, 2025
GenoGenix LLC
Alpha Lipoic Acid for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Lack of Assurance of Sterility
Class II
Drug Recall · July 30, 2025
GenoGenix LLC
Ascorbic Acid (Vitamin C) for Injection, Preservative Free, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Lack of Assurance of Sterility
Class II