cpsc regulated Recalls

2,143 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA DRUG

Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (High-Risk)

Boothwyn Pharmacy LLC issued a nationwide recall of 186 vials of Semaglutide 2.5 mg/mL injection, 0.8 mL, on July 9, 2025. The FDA enforcement report classifies the recall as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and follow guidance from Boothwyn Pharmacy or a healthcare provider.

Boothwyn Pharmacy
Subpotent Drug
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Health & Personal Care
HIGH
FDA DRUG

Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (4 mL, 2.5 mg/mL)

Boothwyn Pharmacy recalls 648 vials of semaglutide 2.5 mg/mL injection nationwide after detecting subpotent potency. The recall involves products distributed across the U.S. and is classified as Class II with a high hazard level. Stop using the product and contact Boothwyn Pharmacy or a healthcare provider for guidance.

Boothwyn Pharmacy
Subpotent Drug
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Health & Personal Care
HIGH
FDA DRUG

CURAD Alcohol Prep Pads Recall for Subpotent Isopropyl Alcohol (2025)

CURAD Alcohol Prep Pads recalled nationwide after tests found isopropyl alcohol levels subpotent. Medline Industries is the maker listed on recall documents. The issue concerns diluted potency below labeled concentration. Stop using immediately and contact Medline for guidance.

CURAD
Subpotent Drug-
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Health & Personal Care
HIGH
FDA DRUG

Medline Alcohol Prep Pads Recalled for Subpotent Isopropyl Alcohol in 6669874 Units

Medline Industries recalled 6,669,874 units of Alcohol Prep Pads nationwide after detecting subpotent isopropyl alcohol. The pads were distributed nationwide. The recall is classified as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and contact Medline for guidance.

Medline Alcohol Prep
Subpotent Drug-
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Health & Personal Care
HIGH
FDA DRUG

H-E-B inControl Alcohol Pads Recalled for Subpotent Isopropyl Alcohol (2025)

H-E-B and its inControl brand recall 300,000 sterile alcohol pads nationwide after the FDA alerted a subpotent isopropyl alcohol concentration. The pads were packaged in China with components from Taiwan and distributed nationwide. Consumers should stop using the product immediately and seek guidance from healthcare providers or MEDLINE INDUSTRIES, LP.

H-E-B
Subpotent Drug-
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Food & Beverages
HIGH
FDA FOOD

Evergreen Orchard Farm Grape Juice Recalled in 78 Cases for 2025 Pasteurization Lapse

Evergreen Orchard Farm recalled 78 cases of Grape Juice in 4 oz foil pouches distributed to PA, NJ and NY. The recall cites lack of pasteurization and sanitation records. Consumers who purchased the product should not consume it and should contact Evergreen Orchard Farm, LLC via Email for refund or replacement.

Evergreen Orchard Farm
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Recalling 19 Units of t:slim X2 Insulin Pump Over RTL App Defect (2025)

Tandem Diabetes Care recalls 19 units of the t:slim X2 insulin pump with interoperable technology distributed internationally, including Israel. An app defect occurs when the phone uses a right-to-left language and can cause app-pump pairing problems and graphical defects. Patients should stop using the device immediately and follow the manufacturer’s recall instructions.

Tandem Diabetes Care
an app
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Health & Personal Care
HIGH
FDA DEVICE

North American Rescue JETT Medical Device Recall for Lower-Limb Occlusion Tool (2025)

North American Rescue recalled 552 units of the JETT device, used for occlusion of blood flow to the lower limbs, due to a manufacturing defect that may compromise structural integrity and performance. The recall covers multiple kits distributed worldwide, including U.S. states and several international countries. Stop using the device immediately and await recall instructions from the company or

North American Rescue
Device used
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Vehicles & Parts
HIGH
NHTSA

VOLKSWAGEN Atlas Recall 2025 for Service Brakes Bolts in Atlas, Atlas Cross Sport, ID.4

Volkswagen Group of America recalls 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 models for loose bolts in the chassis, brake system and suspension. The potential consequence is loss of vehicle control and a crash risk. Owners should stop driving the vehicle and contact a dealer for inspection; recall letters were mailed on July 25, 2025.

Volkswagen
A loss
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Vehicles & Parts
HIGH
NHTSA

Honda 2025 CR-V Hybrid Recall for Fuel Hose Installation Could Cause Fire (TLS)

Honda recalls 2025 CR-V Hybrid vehicles sold through Honda dealers nationwide after finding an improperly installed fuel feed hose that may leak. The recall is identified by Honda as TLS. Dealers will replace the fuel feed hose and install a new connector cover at no charge. Owners should contact Honda at 1-888-234-2138 for service.

Honda
A fuel
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Vehicles & Parts
HIGH
NHTSA

Ford recalls 2025 Expedition air bags for passenger-side deployment risk

Ford Motor Company recalls certain 2025 Expedition and Navigator vehicles due to a passenger-side frontal air bag that may deploy with excessive force. Dealers will replace the passenger side air bags at no charge. Owner notification letters were mailed August 8, 2025.

Ford Motor Company
An air
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Health & Personal Care
HIGH
FDA DEVICE

bioMerieux VITEK 2 AST Cards Recalled for False Colistin Results (235,269 Cards) 2025

bioMerieux recalled 235,269 VITEK 2 Gram-negative AST test cards containing Colistin cs02n, distributed internationally. The cards may produce false resistant results for Colistin when testing certain multi-drug-resistant bacteria. Healthcare providers should stop using the affected cards immediately and follow the recall instructions from bioMerieux.

bioMerieux
Potential for
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Vehicles & Parts
HIGH
NHTSA

GM Recalls 2024-2025 Chevrolet Blazer EV for Parking Brake Wiring Harness Issue

GM recalls 2024-2025 Chevrolet Blazer EVs due to a rear parking brake wiring harness that may corrode or become damaged. The defect can cause unintended parking brake activation or loss of function, increasing crash risk. Dealers will inspect and reroute the harness, install anti-abrasive tape, and replace damaged harnesses at no cost. Owner notices mailed October 1, 2025. Contact Chevrolet at 1-[

CHEVROLET
Unintended activation
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Food & Beverages
HIGH
FDA FOOD

BulkSupplements.com Inositol Recall Affects 1,001 Units Over Possible Staphylococcus Contamination (

BulkSupplements.com recalled 1,001 units of Inositol powder sold in the U.S. and abroad after potential contamination with Staphylococcus aureus. The finished product was distributed by Hard Eight Nutrition LLC dba BulkSupplements.com and classified as a Class II recall. Consumers should stop using the product and seek refunds or replacements from the company.

BulkSupplements.com
Finished product
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Health & Personal Care
HIGH
FDA DEVICE

Orthofix Pillar SA Ti Spinal Implant Recalled for Labeling Error (2025)

Orthofix U.S. recalled 3 Pillar SA Ti intervertebral body fusion devices nationwide in the United States after a labeling discrepancy. The 37 mm implant width is correct on the front label, but the outer side flap and inner label information box incorrectly state 33 mm. Healthcare providers and patients should stop using the device immediately and await manufacturer instructions.

Orthofix U.S.
A 37
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Health & Personal Care
HIGH
FDA DEVICE

Quidel Dipstick Strep A Tests Recalled for Potential False Positives (Z-2545-2025)

Quidel recalls 22,470 Rapid Strep A Dipstick tests sold worldwide, including multiple U.S. states. The dipstick test may yield false positive results. Health providers and patients should stop using the device immediately and follow recall instructions. Check with Quidel for refund or replacement options.

Quidel
Dipstick strep
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Tag Statistics

Total Recalls
2,143

Related Tags

toddler productadult productchemical hazardpoisoning riskimmediate actionreturn for refundfederal law violationnhtsa regulatedelectrical hazardburn riskinfant productstop use immediately