Safety Recalls

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

Showing 201–250 of 15,768

• Consumer Product Recall · July 9, 2026

  iDecoz Inc. dba Flaunt, of Brooklyn, New York

  Flaunt MagSafe Battery Chargers

  The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards.

  Unclassified

• Consumer Product Recall · July 9, 2026

  shenzhenshiyuezhangwangluokejiyouxiangongsi (Shenzhen Yuezhang Network Technology Co., Ltd.), doing business as YUEZHANG, of China

  Moodooy Adult Portable Bed Rails

  The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.

  Unclassified

• Food Recall · July 8, 2026

  Green Jeeva LLC

  Organic Moringa Powder; 15kg/bag (bulk); Product code: GJ96

  Moringa Powder ingredient positive for salmonella

  Class I

• Drug Recall · July 8, 2026

  Ascend Laboratories, LLC

  Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC., Parsnippany, NJ 07

  Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications

  Class II

• Food Recall · July 8, 2026

  Man Fon, Inc.

  Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz; UPC# 757168 977315, Keep Refrigerated, Can be Frozen. Sold in 48 units (10oz)/case.

  Undeclared colors: Yellow#5, and Yellow#6.

  Class II

• Food Recall · July 8, 2026

  Man Fon, Inc.

  Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units (16oz bags)/case. Wonton Wrappers packed into "Wonton Noodles Net Wt. 5 LBS" plastic bags and sold as 10 units (4-lb bags)/

  No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6.

  Class II

• Vehicle Recall · July 7, 2026

  Tesla, Inc.

  2024 TESLA MODEL 3

  A noncompliant vehicle may have reduced occupant protections, increasing the risk of injury during a crash.

  Unclassified

• Medical Device Recall · July 7, 2026

  INTEGRATED MEDCRAFT LLC

  FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050.

  Devices could potentially contain an occluded or partially occluded Guedel Airway tip.

  Class II

• Vehicle Recall · July 7, 2026

  Subaru of America, Inc.

  2023 SUBARU ASCENT, 2024 SUBARU ASCENT, 2025 SUBARU FORESTER, 2025 SUBARU ASCENT

  An incorrect GAWR label may lead to an overloaded vehicle, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · July 7, 2026

  INTEGRATED MEDCRAFT LLC

  Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. 2. Size 000, IS

  Devices could potentially contain an occluded or partially occluded Guedel Airway tip.

  Class II

• Medical Device Recall · July 7, 2026

  Olympus Corporation of the Americas

  Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.

  Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.

  Class II

• Medical Device Recall · July 6, 2026

  Waldemar Link GmbH & Co. KG (Mfg Site)

  Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16

  The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as the plateau cannot be inserted and an alternative product would be needed. If the incorrect plateau were to be implanted, this is associated with increased risk of wear, which could result in a reduced standing time of the implant.

  Class II

• Drug Recall · July 6, 2026

  Supernus Pharmaceuticals, Inc.

  Trokendi XR, topiramate extended-release capsules, 25mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., R

  Failed Dissolution Specifications

  Not Yet Classified

• Medical Device Recall · July 6, 2026

  Spectra Medical Devices, Llc

  Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride Flush for IV tubing systems and ind

  Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients may be exposed to microorganisms, endotoxins, or foreign matter. This may trigger inflammatory responses, infections, micro-clots, and organ failure.

  Class I

• Drug Recall · July 6, 2026

  Supernus Pharmaceuticals, Inc.

  Trokendi XR, topiramate extended-release capsules, 25mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., R

  Failed Dissolution Specifications

  Class III

• Drug Recall · July 6, 2026

  Chiesi USA, Inc.

  CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials, Rx Only, Manufactured for: Chiesi USA, Inc., Cary, NC 27518, by Fresenius Kabi, Graz, Austria, NDC 10122-611-

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 6, 2026

  Siemens Healthcare Diagnostics, Inc.

  Atellica CH Urine Albumin REF: 11537225, in vitro diagnostic

  Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed Atellica CH Enzymatic Hemoglobin A1c (A1c_E) results; Increased rate of reaction cuvette QC failures and Delayed results due to QC failures.

  Class II

• Vehicle Recall · July 5, 2026

  General Motors, LLC

  2026 CADILLAC ESCALADE, 2026 CADILLAC ESCALADE ESV, 2026 CHEVROLET SILVERADO 1500, 2026 CHEVROLET TAHOE, 2026 GMC SIERRA 1500, 2026 GMC YUKON, 2026 GMC YUKON XL

  Front or rear wheel lockup increases the risk of a crash.

  Unclassified

• Vehicle Recall · July 5, 2026

  Chrysler (FCA US, LLC)

  2023 JEEP CHEROKEE

  A failed PTU may result in a loss of drive power or vehicle rollaway, increasing the risk of a crash or injury.

  Unclassified

• Food Recall · July 3, 2026

  Frutas y Hortalizas del Sur S.A.

  Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen

  Potential E. coli O145:H28 Contamination

  Class I

• Consumer Product Recall · July 2, 2026

  Groupe SEB USA dba Rowenta USA, of Parsippany, New Jersey

  Rowenta Cordless Vacuum Cleaners with lithium-ion battery

  The recalled lithium-ion battery in the vacuum cleaner can overheat and ignite, posing a risk of serious injury from fire and burn hazards.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Xishentang Dongguan Trading Co, Ltd., dba Pretty-Life, of China

  AMASKY Nursing Pillows

  The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support cushions because they can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Conair LLC, of Stamford, Connecticut

  Metal Wire Bristle Grill Brushes

  Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Sanven Technology Ltd., dba Vevor, of Rancho Cucamonga, California

  VEVOR baby loungers

  The recalled baby loungers violate the mandatory safety standard for infant sleep products. The sides are too low to contain an infant and the enclosed openings at the foot of the loungers are wider than allowed, posing serious risks of fall and entrapment hazards to infants. In addition, the baby loungers do not have a stand, posing a fall hazard if used on elevated surfaces. These violations create an unsafe sleeping environment and can cause death or serious injury.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Changsha Jiali Duo Technology Co., Ltd., dba Topyond, of China

  Topyond Pool Drain Port with Cover

  The recalled drain ports with covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to consumers.

  Unclassified

• Drug Recall · July 2, 2026

  MYLAN PHARMACEUTICALS INC

  Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India, NDC 67457-386-

  Presence of precipitate

  Class II

• Consumer Product Recall · July 2, 2026

  Changzhou Niujie Battery Technology Co., Ltd., dba JSNJ_Tech, of China

  Junpower CR2032 Batteries

  The lithium coin batteries are not sold in child-resistant packaging and do not bear the warning labels as required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns and death.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Shenzhen Bopu Product Design Co., Ltd., dba POPOOO, of China

  POPOOO Jungle Safari LED Finger Lights

  The recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Cooper Lighting, LLC, of Peachtree City, Georgia

  Metalux Optimized High Bay (OHB) LED Light Fixtures

  The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Diamond Wipes International, Inc. of Chino, California

  CVS Health Medicated Hemorrhoidal Wipes

  The recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not child-resistant, posing a risk of serious injury or death from poisoning if the contents of the wipes are ingested by young children.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Winco Fireworks International, LLC, of Grandview, Missouri

  Unity 7 Shot 200 Gram Aerial Cake Firework Devices

  The recalled fireworks can tip over, posing a risk of serious injury from explosion and burn hazards.

  Unclassified

• Medical Device Recall · July 2, 2026

  IsoTis OrthoBiologics, Inc.

  OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095

  Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc DBM (fill for 45 ¿ 11 mm configuration) instead of approx. 7.5 cc DBM (fill for 45 ¿ 17.5 mm configuration), which may lead to delayed fusion, incomplete fusion, pseudarthrosis, or lack of bone ingrowth.

  Class II

• Food Recall · July 2, 2026

  Brooklyn Roasting Works LLC

  Brooklyn Roasting Company Pasteurized Cold Brew Concentrate; 2.5gal; bag in a box distributed between 04/01/2026 and 06/20/2026.

  Ambient storage of the product may lead to Clostridium botulinum toxin formation.

  Class II

• Consumer Product Recall · July 2, 2026

  Target, of Minneapolis, Minnesota

  Gigglescape™ Under the Sea Popping Toy

  The clear plastic dome can detach from the blue plastic base, making the small plastic balls inside the toy accessible to children, posing a choking hazard.

  Unclassified

• Consumer Product Recall · July 2, 2026

  Winco Fireworks International, LLC, of Grandview, Missouri

  Roman Candles 8 Shot 3-Pack Firework Devices

  The recalled fireworks can malfunction, and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards.

  Unclassified

• Food Recall · July 1, 2026

  Eunha Fisheries Co., LTD

  FLOUNDER SASHIMI WITH SAUCE; Keep Frozen; Net WT: 300g; UPC: 8 809342 366186

  Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.

  Class II

• Medical Device Recall · July 1, 2026

  Stryker GmbH

  Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060.

  Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

  Class II

• Food Recall · July 1, 2026

  Eunha Fisheries Co., LTD

  Sliced Korean Halibut with Soy sauce, Wasabi, Vinegar Chili Paste; Keep Frozen; Net WT: 12.2OZ (374g); UPC: 6 78108 16991 4

  Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.

  Class II

• Medical Device Recall · July 1, 2026

  Aniara Diagnostica LLC

  5-PLASMA Bivalirudin Control, Model Number 5D-44905

  Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values.

  Class II

• Medical Device Recall · July 1, 2026

  Biomet, Inc.

  Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blade Assembly 14mm

  Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

  Class II

• Medical Device Recall · July 1, 2026

  Aniara Diagnostica LLC

  5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905

  Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values.

  Class II

• Medical Device Recall · July 1, 2026

  Stryker GmbH

  Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.

  Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

  Class II

• Medical Device Recall · July 1, 2026

  Biomet, Inc.

  Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade Assembly 13mm

  Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

  Class II

• Medical Device Recall · July 1, 2026

  Biomet, Inc.

  Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade Assembly 12mm

  Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

  Class II

• Drug Recall · July 1, 2026

  Victory Medical Center Pharmacy

  Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VMC.

  Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

  Class I

• Medical Device Recall · July 1, 2026

  Stryker GmbH

  Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.

  Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

  Class II

• Medical Device Recall · July 1, 2026

  Biomet, Inc.

  Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product Description: Intramedullary Bone Saw Blade Assembly 16mm

  Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

  Class II

• Food Recall · July 1, 2026

  JINA F&C

  Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium Soybean Paste UPC: 8 809897 940169

  Product label allergen "contains" statement does not include anchovy(fish)

  Class II

• Medical Device Recall · July 1, 2026

  Stryker GmbH

  Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.

  Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

  Class II

• Medical Device Recall · July 1, 2026

  Stryker GmbH

  Stryker Hoffmann II Connecting Rod Micro 3 x 120mm. Catalog Number: 50796120.

  Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

  Class II