chemical hazard Recalls

1,035 recalls tagged with “chemical hazard”.

Recalled GM Gumili Wintergreen Essential Oil-Bottle and Box Front
HIGH
CPSC

GM Gumili Wintergreen Essential Oil Recalled for Child Poisoning Risk

GM Gumili recalled its Wintergreen Essential Oil on February 6, 2026, after it was found to lack child-resistant packaging. The essential oil contains methyl salicylate, which poses a risk of poisoning to young children if ingested. Consumers should stop using the product immediately and return it for a full refund.

GM Gumili Wintergreen Essential Oil Bottles
The essential
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Compounding Issues Recall of Vancomycin Injection

Fresenius Kabi Compounding recalled 1,578 bags of vancomycin HCl injection on February 5, 2026. The company cited a lack of assurance of sterility as the reason for the recall. Healthcare providers and consumers should stop using the product immediately.

Fresenius Kabi Compounding
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Compounding Recalls Ketamine Injection for Sterility Risk

Fresenius Kabi Compounding recalled 1,410 bags of ketamine HCl injection on February 5, 2026. The recall stems from a lack of assurance of sterility, posing a high health risk. Healthcare providers and consumers must stop using this product immediately.

Fresenius Kabi Compounding
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Compounding Recalls Thiamine Injection Over Sterility Risk

Fresenius Kabi Compounding recalled 10,548 bags of thiamine HCl injection on February 5, 2026. The recall follows a lack of assurance of sterility, posing a high health risk. Affected products include several lots expiring between February and May 2026.

Fresenius Kabi Compounding
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Remel Recalls Campy CVA Medium Over Low Recovery Rates

Remel, Inc. recalled 97 units of Campy CVA Medium on February 5, 2026. Customers reported low to no recovery of Campylobacter Jejuni ATCC 33291 in the affected lot. Healthcare providers and patients must stop using the product immediately.

Remel
Customer complaints
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Recalled EnHomee 10 drawer dresser (front)
HIGH
CPSC

EnHomee 10-Drawer Dressers Recalled for Tip-Over Hazard (2026)

EnHomee recalled its 10-Drawer Dressers sold on Amazon after determining tip-over and entrapment hazards. The recall also notes a violation of the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and contact EnHomee for a full refund.

EnHomee
The recalled
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Recalled LOTUSJOY Sweet Birch Essential Oil - Packaging, Bottle and Glass Dropper
HIGH
CPSC

Zan International Trading Recalls Lotus Joy Sweet Birch Essential Oil Packaging (2026)

Zan International Trading recalls Lotus Joy Organic Sweet Birch Essential Oil bottles due to packaging that is not child-resistant. The product contains methyl salicylate and poses a poisoning risk to children if swallowed. Stop using the product now and return it for a full refund by contacting Zan International Trading.

Zan International Trading
The essential
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Food & Beverages
HIGH
FDA FOOD

Pure Solutions Recalls Sleep Formula Over Milk Allergen Risk

Pure Solutions recalled 442 bottles of its sleep supplements on February 3, 2026. The labels did not declare a milk allergen despite containing bovine colostrum. Consumers should stop using the product immediately and seek refunds.

Pure Solutions
Label declares
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Health & Personal Care
HIGH
FDA DRUG

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Deviations

Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.

PRO NUMB
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Violations

Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.

PRO NUMB SENSITIVE SKIN
cGMP deviations
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Food & Beverages
HIGH
FDA FOOD

Costco Recalls Mini Beignets Due to Undeclared Hazelnut

Costco recalled 8,073 packages of Kirkland Signature Mini Beignets on January 31, 2026. The products contain undeclared hazelnut, posing a serious risk to those with allergies. The beignets were distributed in multiple states including California and Texas.

Costco Wholesale
Undeclared hazelnut.
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Food & Beverages
HIGH
FDA FOOD

Reser's Tuna Salad Recalled Over Undeclared Fish Allergen

Reser's Fine Foods recalled 298 tubs of Tuna Salad on January 30, 2026 due to undeclared fish allergens. The product was mislabeled with a Chicken Salad lid, posing a risk to consumers with fish allergies. The recall affects distribution in Arizona, California, Nevada, Utah, and Washington.

Reser's Fine Foods
Undeclared fish
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Recalled Bazic Silicone Glue – Front and Side
HIGH
CPSC

Bazic Products Recalls Silicone Glue Over Child Poisoning Risk

Bazic Products recalled Bazic Silicone Glue on January 29, 2026, due to a serious poisoning risk for children. The glue's packaging does not meet child-resistant standards, violating federal law. Consumers should stop using the product immediately and seek a full refund.

Bazic Products
The glue
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Recalled VIOFAIRY Hair Growth Serum bottle and packaging
HIGH
CPSC

Viofairy Hair Growth Serum Recalled Over Child Poisoning Risk

Viofairy recalled its Hair Growth Serum on January 29, 2026, due to serious poisoning risks. The packaging lacks required child-resistant features, endangering young children. Consumers must stop using the product immediately and secure it out of reach.

Guangzhou Runshu BioTech Co., Ltd. of China
The serum
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Food & Beverages
HIGH
FDA FOOD

Preema Food Colour Powder Recalled Over Banned Ingredients

Preema brand recalled 720 bottles of Bright Red and Orange Food Colour Powders on January 29, 2026. The products contain a banned color, carmoisine, and undeclared FD&C Yellow 5 and FD&C Red 40. Consumers should not consume these products and seek refunds immediately.

KPCM New York
Products contain
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate ER 100 mg Recall Expanded for Failed Dissolution Specifications (2026)

Teva Pharmaceuticals recalled 7,448 bottles of Metoprolol Succinate Extended-Release Tablets nationwide after failed dissolution specifications were identified. The recall involves 100 mg, 100‑tablet bottles (NDC 45963-677-11) and 1,000‑tablet bottles (NDC 45963-677-96). The defect may affect drug release and efficacy. Patients should stop using affected bottles and contact Teva or their clinician

METOPROLOL SUCCINATE
Failed Dissolution
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Food & Beverages
HIGH
FDA FOOD

Koi Koi Trading Recalls Fish Balls Over Allergen Risk

Koi Koi Trading recalled 8,232 cases of frozen fish balls on January 28, 2026. The product contains undeclared wheat and sesame allergens, posing a serious health risk. Consumers should check their freezers and take immediate action.

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING
Undeclared allergen
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