chemical hazard Recalls

1,003 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DRUG

Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency; 49,275 Tubes Affected

FDA-listed recall covers 49,275 tubes sold nationwide. Ultra Violette Velvet Screen Blurring Mineral Skinscreen distributed by Grace & Fire USA Inc. Tested SPF results ranged from 4 to 64. Consumers should stop using the product immediately and contact Grace & Fire USA for guidance.

ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN
Subpotent/Super-potent Product:
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle

CooperVision recalled one lot of Voyant 1-Day Premium Toric contact lenses sold nationwide in the United States after an invalid sterilization cycle was detected. The recall affects 90 units distributed in Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the lenses immediately and contact their eye care professional for guidance.

CooperVision
One lot
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Health & Personal Care
HIGH
FDA DEVICE

Frontier Devices 301.912S1 12 mm Distraction Pin Recall Expanded to 3,790 Units (Rx Only)

Frontier Devices recalled 3,790 units of the 12 mm Distraction Pin, REF 301.912S1, distributed nationwide in the United States. The recall cites labeling that includes shelf life which has not been validated. The high-risk device category reflects potential documentation and shelf-life concerns. Healthcare providers and patients should follow recall instructions and contact the manufacturer for a回

Frontier Devices
Labeling includes
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Food & Beverages
HIGH
FDA FOOD

Taylor Farms Retail Salad Kit Recalled for Undeclared Sesame and Soy Allergens (2025)

Taylor Farms Retail issued a Class I recall for 8,284 salad kits after undeclared sesame and soy allergens were found inside a dressing packet. The recall covers products labeled under Taylor FARMS Honey Balsamic Salad Kit sold across 19 states. Consumers should not eat the product and should seek refunds or replacements from Taylor Farms Retail.

Taylor Farms Retail
Undeclared allergens
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Health & Personal Care
HIGH
FDA DEVICE

Abbott i-STAT CG4+ Cartridge Recall: 9,067,050 Units Across U.S. With 510(k) Clearance Issue (2025)

Abbott Point Of Care recalled 9,067,050 i-STAT CG4+ cartridges sold nationwide in the United States. The recall cites a lack of 510(k) premarket clearance to reflect updated sample type for lactate and measurement ranges for pH and PO2. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.

Abbott Point Of Care
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Frontier Devices 301.916S1 16 mm Distraction Pin Recall Expanded (2025)

Frontier Devices and Folsom Metal Products issued a high-risk recall for 490 units of the 16 mm Distraction Pin, REF 301.916S1, distributed nationwide in the United States. The labeling includes shelf life that has not been validated. Patients and healthcare providers should stop using the device immediately and follow recall instructions.

Frontier Devices
Labeling includes
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Vehicles & Parts
HIGH
NHTSA

Chevrolet Corvette 2025 Recall for Fuel System Fire Risk After Refueling Spill

Chevrolet Corvette owners are being notified by General Motors dealers to fix a fuel-spill risk in 2023–2026 Corvette models. During refueling, excess fuel may spill into the vehicle fuel-filler pocket and reach an ignition source, increasing fire risk. Dealers will install a shield at no charge. Letters were mailed Sept. 10, 2025. Owners should contact Chevrolet customer service at 1-800-222-1020

Chevrolet
A fuel
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Health & Personal Care
HIGH
FDA DRUG

Baxter Acetaminophen Injection 1000 mg/100 mL Recall for Discoloration

Baxter Healthcare’s Acetaminophen Injection 1000 mg/100 mL is recalled. The nationwide recall covers 13,000 containers with lot 24A27G66 and expiring 12/31/2025. The FDA lists discoloration as the hazard. Stop using and contact Baxter or a healthcare provider.

Baxter Healthcare Corporation
Discoloration
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Health & Personal Care
HIGH
FDA DRUG

96 Bottles of Sulfamethoxazole and Trimethoprim Tablets Recalled for Micro-Organism Contamination

Northwind Pharmaceuticals recalled 2,295 bottles of Sulfamethoxazole and Trimethoprim Tablets due to contamination risks. A foreign substance was detected in the packaging's auxiliary polyester coil, although no micro-organisms were found on the tablets. Consumers should stop using these products immediately and contact Northwind Pharmaceuticals for guidance.

SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
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Food & Beverages
HIGH
FDA FOOD

Itacate Foods CAMPSITE LENTEJAS Lentil Soup Recalled for Undeclared Yellow Dyes (154 Packages, 2025)

Itacate Foods recalled 154 packages of CAMPSITE LENTEJAS lentil soup sold in the United States after undeclared Yellow #5 and Yellow #6 were detected on the label. The issue involves undisclosed food color additives that could trigger allergic reactions in sensitive individuals. Consumers should discard the product and contact Itacate Foods for a refund or replacement.

Itacate Foods
Undeclared Yellow
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recall 28,911 U128 ACCOLADE, VISIONIST VALITUDE CRT-P Devices (2025)

Boston Scientific recalled 28,911 pacemakers worldwide due to a software flaw in Safety Architecture that could prevent Safety Mode when battery impedance is high. The recall covers ACCOLADE family devices and VISIONIST and VALITUDE CRT-Ps. Patients should stop using the device immediately and follow the recall letter instructions.

Boston Scientific
Software to
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Food & Beverages
HIGH
FDA FOOD

Best Yet, Arctic Shores, and Great American Frozen Shrimp Recalled for Cs-137 Contamination (2025)

Best Yet, Arctic Shores, and Great American frozen shrimp were recalled by Southwind Foods LLC dba Great American Seafood Imports Co. The recall cites insanitary production conditions that may have contaminated products with Cesium-137. Consumers who purchased these products should not consume them and should contact the company for refunds or replacements.

Best Yet
Product manufactured
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Tag Statistics

Total Recalls
1,003

Related Tags

choking hazardburn risksuffocation riskstop use immediatelyreturn for refundreplacement availableimmediate actioncpsc regulatedfda regulatedbattery poweredlithium batteryinfant product