chemical hazard Recalls

1,079 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Stryker Communications Recalls 40 Medical Light Systems Over Powder Coating Chip Risk (2025)

Stryker Communications recalls 40 surgical light systems nationwide after reports of stress lines in the powder coating. The devices include CH00000001 and the SLX to Oculan NFC Upgrade Kit, P60034. The recall is active as of July 15, 2025. Patients and healthcare providers should stop using the devices immediately and follow manufacturer recall instructions.

Stryker Communications
Surgical lights
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Recalled SPPTTY Kids 14-inch Bicycle in Pink
HIGH
CPSC

SPPTTY Kids Bicycles Recalled for Lead Poisoning Risk (2025)

SPPTTY recalled kids bicycles sold at Walmart after lead levels exceeded the federal lead content ban in multiple components and on the black paint used on pumps. The recall urges consumers to stop using the bicycles immediately. To receive a refund, dismantle the bicycles, photograph the setup, and email the photo to lishkjie@163.com; after destruction is verified, dispose of the bike.

SPPTTY
Multiple components
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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

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

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

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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Health & Personal Care
HIGH
FDA DRUG

Rite Aid Alcohol Prep Pads Recalled Over Subpotent Isopropyl Alcohol Levels (2025)

Rite Aid alcohol prep pads distributed nationwide are recalled after subpotent isopropyl alcohol levels were found below label concentration. Medline Industries, LP notified distributors and healthcare providers in a Class II recall dated July 7, 2025. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare provider.

Rite Aid
Subpotent Drug-
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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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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Deep Sprouted Mat 16 oz Recalled for Salmonella Risk 2025

CHETAK NEW YORK LLC recalled 5,232 packets of Deep Sprouted Mat 16 oz distributed to California, New Jersey, Illinois, Florida and Texas after tests found Salmonella. The recall class is I with a high hazard level. Consumers should not consume the product and should seek refund or replacement by email.

CHETAK NEW YORK
Product tested
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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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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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Food & Beverages
HIGH
FDA FOOD

Nirwana Foods Golden Raisin Recalled for Undeclared Sulfites in 28 oz Bags (2025)

Nirwana Foods recalled Golden Raisin sold in New Jersey and New York after undeclared sulfites were detected. The packaging did not declare sulfites. Consumers should not consume the product and should contact Nirwana Foods LLC for refund or replacement information using one of several notification methods.

Nirwana Foods
Undeclared Sulfites
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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
1,079

Related Tags

electrical hazardsuffocation risktip over riskinfant productadult productburn riskstop use immediatelyreturn for refundfda regulatedcpsc regulatednhtsa regulatedpoisoning risk