adult product Recalls

989 recalls tagged with “adult product”.

Food & Beverages
HIGH
FDA FOOD

Extract Labs Mai Tai 20mg Gummies Recalled for Peanut Cross-Contact Risk (2025)

Extract Labs recalled 19,750 Mai Tai 20mg Gummies distributed across the United States, Australia, Germany, the United Kingdom, Malaysia and New Zealand. The unlabeled bulk product was shipped in poly gusset bags inside brown corrugated boxes with no consumer label. Consumers who bought it should not consume the product and should email Extract Labs to request a refund or replacement.

Extract Labs
Potential peanut
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Health & Personal Care
HIGH
FDA DEVICE

GORE ACUSEAL Vascular Graft Recall Affects 52,306 Devices Worldwide (2025)

Gore recalled 52,306 Gore ACUSEAL Vascular Grafts distributed through healthcare providers in the United States and internationally after reports of graft delamination. Delamination may reduce access flow, cause cannulation difficulties, bleeding or bruising, and may require reinterventions. Healthcare facilities and patients should stop using the device immediately and follow the recall guidance.

Gore
Reports of
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Health & Personal Care
HIGH
FDA DRUG

Kroger 70% Isopropyl Alcohol Recall Expands for Cross-Contamination Risk

Kroger 70% isopropyl alcohol recall active nationwide, 1860 bottles involved. The recall covers Kroger-branded rubbing alcohol distributed by The Kroger Co. No injuries are reported in the notice. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare professional.

Kroger
Cross Contamination
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Health & Personal Care
HIGH
FDA DRUG

AvKare Chlorpromazine Hydrochloride 50 mg Tablets Recalled for Foreign Substance Contamination (2025

AvKare recalled 1,512 cartons of CHLORPROMAZINE HYDROCHLORIDE 50 mg tablets distributed nationwide in the U.S. for the presence of a foreign substance. The recall is active as of Sept. 17, 2025. Consumers and healthcare providers should stop using this product immediately and contact AvKARE or a healthcare provider for guidance.

AvKare
Presence of
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Health & Personal Care
HIGH
FDA DEVICE

LeMaitre Vascular Artegraft 10-Unit Recall 2025 for Labeling Errors

LeMaitre Vascular recalls 10 Artegraft Collagen Vascular Grafts distributed internationally to Great Britain and Switzerland, with no US distribution. The devices were labeled incorrectly and lacked CE and UKCA marks and missing patient documents. Healthcare providers and patients should stop using the devices and follow recall instructions immediately.

LeMaitre Vascular
Devices were
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Vehicles & Parts
HIGH
NHTSA

Ford Recalls 2025 Explorer and Aviator for Trailer Tail Light Failure (25C42)

Ford recalls 2025 Explorer and Aviator vehicles sold through Ford dealers due to a faulty body control module that can prevent trailer tail lights from illuminating. The defect may reduce visibility for other drivers when towing a trailer. Interim letters alert owners starting Oct 13, 2025, with a final remedy anticipated in April 2026. Ford will perform the repairs at no charge and provide the an

Ford
Trailer tail
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Recalls 180 Softmed Breathables Toric Lenses Over Invalid Sterilization Cycle (2025)

CooperVision recalled 180 Softmed Breathables toric daily disposable contact lenses after one lot was manufactured with an invalid sterilization cycle. The lenses were distributed across Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the affected lenses immediately and follow the recall instructions.

CooperVision
One lot
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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 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

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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Tag Statistics

Total Recalls
989

Related Tags

immediate actionreturn for refundelectrical hazardchemical hazardstop use immediatelysuffocation riskinfant producttoddler productelderly productcpsc regulatedfda regulatedbattery powered