Safety Recalls

15,768 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 151–200 of 15,768

• Medical Device Recall · July 16, 2026

  Biofire Defense

  FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: (01)00851458005136 The FilmArray NGDS Warrior Panel is a qualitative, multiplexed, nucleic acid-based in vitro diagnostic test intended

  Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic acid-based in vitro diagnostic panel test.

  Class II

• Drug Recall · July 16, 2026

  Fresenius Kabi USA, LLC

  Naropin (ropivacaine hydrochloride Injection, USP), 0.5%, 100 mg per 20 mL (5 mg per mL), Twenty-five, 20 mL Single-Dose Vials, Rx only, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-286-23; N

  Presence of Particulate Matter: Hair was found in products

  Class II

• Medical Device Recall · July 16, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software Version Numbers: R3.0 and R3.1; Interventional fluoroscopic x-ray system

  Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications

  Class II

• Consumer Product Recall · July 16, 2026

  J. Crew Group, LLC of New York, New York

  Madewell Double V-Neck Pullover and V-Neck Cardigan Sweaters

  The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death.

  Unclassified

• Drug Recall · July 16, 2026

  Fresenius Kabi USA, LLC

  Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5 mL per vial, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-208-05; NDC Vial: 63323

  Presence of Particulate Matter: Hair was found in products

  Class II

• Consumer Product Recall · July 16, 2026

  Target, of Minneapolis, Minnesota

  Cat & Jack Children's Sandals

  The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard.

  Unclassified

• Medical Device Recall · July 16, 2026

  Straumann USA LLC

  Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form

  Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest.

  Class II

• Food Recall · July 16, 2026

  CHEER PACK

  Flexible food pouch (3-layer foil, spouted, #CP6088), manufactured for packaging Pumpkin Tree Peter Rabbit Organics Banana & Strawberry, 4 oz food puree, UPC 815367010780.

  Flexible food pouch may release thin plastic strips into food.

  Class II

• Drug Recall · July 15, 2026

  Asclemed USA Inc.

  Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 76420-760-01.

  Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan

  Class III

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, TWIN PACK 0.34 FL OZ (10 mL) each, Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, U

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog Number: SEN21SPPMB

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Drug Recall · July 14, 2026

  Precision Dose Inc.

  Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc, S. Beloil, IL 61080, unit-dose oral syringes, NDCs 68094-073-01 (oral syringe) and 68094-073-58 (case).

  Failed Impurities/Degradation Specifications

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO , Cata

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) SEPTO RHINO PACK , Catalog Number: SEN73NSKCF; 2) PACK NEURO MINOR CRANIOTOMY , Catalog Number: SNE30CNOHE; 3) NEURO MAJOR 2 PACK , Catal

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 80 0.2%), Sterile, TWIN PACK, 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Mad

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT , Catalog Number: 21-4720B; 2) TRAY FAT GRAFT ADD , Catalog Number: 21-4720C; 3) KIT,BOSC MICROLARYNGOSCOPY , Catalog N

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Cool Relief (naphazoline hydrochloride 0.012%, polysorbate 80 0.2%), Sterile, 0.4 FL OZ (13 mL) each, Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in V

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC27; 2) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC28; 3) CHI STD NEURO CRANI OPT 2 , Catal

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Digi Eye (hypromellose 0.35%, tetrahydrozoline HCl 0.05%), Sterile, 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310

  Lack of Assurance of Sterility

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, 0.34 FL OZ (10 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011135

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK , Catalog Number: SNE11SPHKC; 3) SPINE PACK , Ca

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 90, 0.2%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietn

  Lack of Assurance of Sterility

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Optic Glow (naphazoline hydrochloride 0.03%, povidone 0.5%, propylene glycol 0.2%), Sterile, 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127,

  Lack of Assurance of Sterility

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops ALL-IN-ONE (hypromellose 0.2%, tetrahydrozoline HCL 0.05%, zinc sulfate 0.25%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made

  Lack of Assurance of Sterility

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 112 mcg (0.0112 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. N

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Rising Pharma Holding, Inc.

  Rising, Cyproheptadine Hydrochloride Syrup, 2mg/5 mL, 473 mL (ONE PINT), Rx only, Manufactured for: Rising Pharma Holdings, Inc., East Brunswick, NJ, Manufactured by: Lyne Laboratories, Inc., Brockton

  Presence of Precipitate: medication was crystallizing and particles floating in the bottle

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Dist

  Subpotent Drug

  Class II

• Medical Device Recall · July 13, 2026

  Straumann USA LLC

  GM Helix Implant, Endosseous Dental Implant Article No. 109.984

  There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the issue could cause bone compression or difficulty during installation in situations where there is sufficient bone volume

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. N

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distri

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distri

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. N

  Subpotent Drug

  Class II

• Food Recall · July 13, 2026

  PT Organics Limited

  Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720. Distributed by: PT Organics Ltd, 333 South State St, Suite V-142, Lake Oswego, OR

  Possible foreign object (thin, soft plastic strands).

  Class II

• Medical Device Recall · July 13, 2026

  OBP Medical Corporation

  OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1

  There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider.

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distri

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Dist

  Subpotent Drug

  Class II

• Medical Device Recall · July 10, 2026

  GE Medical Systems Information Technologies Inc

  GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system

  A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or access to Protected Health Information (PHI).

  Class II

• Consumer Product Recall · July 9, 2026

  Best Buy Purchasing LLC, of Richfield, Minnesota

  Insignia Front Control Gas Ranges

  The recalled ranges' front-mounted knobs can be activated accidentally by humans or pets, posing a risk of serious injury from a fire hazard.

  Unclassified

• Consumer Product Recall · July 9, 2026

  Jomani International Inc., of Monterey Park, California

  BBRKIN and MouTec Biometric Firearm Safes

  The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.

  Unclassified

• Consumer Product Recall · July 9, 2026

  Zhangzhoushi Jingqu Trading Co., Ltd., dba Wonder Stone Toys, of China

  WonderStone Infant Walkers

  The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall hazard.

  Unclassified

• Consumer Product Recall · July 9, 2026

  Conair LLC, of Stamford, Connecticut, dba Cuisinart

  Cuisinart Propel+ Four Burner 3-in-1 Gas Grill with pizza oven

  The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard.

  Unclassified

• Consumer Product Recall · July 9, 2026

  Greenworks North America, LLC, dba Greenworks Tools, of Mooresville, North Carolina

  Kobalt 24V and 48V Trimmers, Blowers, Mowers, Chainsaws and Pruning Saws with USB-C Batteries

  Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serious injury from fire hazard.

  Unclassified

• Food Recall · July 9, 2026

  Pack'n Fresh LLC

  "***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch, pouches packed in brown paperboard cartons (600 packets/carton), Carton label reads in part as "***Hondashi 0.25oz*600bags/ct

  Allergen missing from contains statement: fish

  Class II

• Drug Recall · July 9, 2026

  CareFusion 213, LLC

  BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0.03fl oz (1 mL) each, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subs

  Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator

  Class II