chemical hazard Recalls

1,035 recalls tagged with “chemical hazard”.

Recalled Arey, Not Today, Grey (180ct) - front
HIGH
CPSC

Vitaquest International Recalls Multiple Iron Supplements for Child-Resistant Packaging Violations (

Vitaquest International recalled Arey Not Today iron supplements sold at retailers nationwide after determining the products do not meet the Poison Prevention Packaging Act's child-resistant packaging requirement. The noncompliant packaging creates a poisoning risk to young children if ingested. Consumers should stop using the products immediately and contact Vitaquest for a free child-resistant替换

Vitaquest International LLC of West Caldwell, New Jersey
The dietary
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Recalled BISSELL Steam Shot OmniReach Steam Cleaner with Attachments
HIGH
CPSC

BISSELL Recalls 1 Million Steam Shot OmniReach Cleaners Over Burn Hazard (2026)

BISSELL recalled more than 1 million Steam Shot OmniReach handheld steam cleaners with attachments, sold nationwide through retailers. The attachments can detach and expel hot water or steam, posing a serious burn hazard. Stop using the attachments immediately and contact BISSELL to receive free replacement attachments.

BISSELL
The recalled
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The article code is marked in the heel area on the inner side of the left boot (Example 601140 shown)
MEDIUM
CPSC

Head USA Recalls Ski Boots for Fall Hazard Risk (2026)

Head USA recalls ski boots with fluorescent yellow components from 2016–2022 model years. The recall covers boots and inserts with six-digit article codes. Consumers should stop using recalled boots immediately and contact Head for a free replacement or sole-insert option.

Head USA
The fluorescent
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Recalled Sam's Club Member's Mark Children's Valentine SS Notch Collar pajama sets
HIGH
CPSC

Sam's Club Recalls Member's Mark Children’s Pajama Sets for Burn Hazard in 2026

Sam's Club recalls Member's Mark Valentine pajama sets due to burn risk and a violation of mandatory flammability standards for children's sleepwear. The recall covers sizes XS through XL sold online between December 2025 and January 2026 for about $14. Consumers should stop using the pajamas immediately and contact Sam's Club for a full refund.

Hansoll Textile Ltd., of South Korea
The recalled
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Recalled Tuymec Minoxidil Hair Growth Serum Spray Bottle (front and back)
HIGH
CPSC

Tuymec Minoxidil Hair Growth Kit Recalled for Non-Child-Resistant Packaging (2026)

Tuymec Minoxidil Hair Growth Kit sold on Amazon by DrHealBeauty is recalled for non-child-resistant packaging. The kit contains two black spray bottles with 5% minoxidil and BIOTIN labels. Consumers should stop using the product immediately and contact DrHealBeauty for a free empty replacement bottle with a child-resistant closure.

Tuymec Minoxidil Hair Growth Spray Bottles
The hair
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Recalled TecFlox Topical Solution - hair and beard growth serum bottle
HIGH
CPSC

TecFlox Minoxidil Topical Solution Hair Serum Recalled for Child Poisoning Risk (2026)

TecFlox recalled its Minoxidil Topical Solution hair growth serum bottles on April 2, 2026. The packaging is not child-resistant, violating the Poison Prevention Packaging Act. Consumers should stop using the product immediately, store it out of reach of children, and email TecFloxrecall@outlook.com to receive free replacement bottles. Only bottles with serum remaining will be replaced; dispose of

TecFlox Hair and Beard Growth Serum Bottles
The hair
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Health & Personal Care
HIGH
FDA DRUG

Biocon Pharma Prazosin Hydrochloride 1mg 100-Count Capsules Recalled for Nitrosamine Impurity (2026)

Biocon Pharma Inc. recalled 88,008 bottles of Prazosin Hydrochloride capsules, 1 mg, 100-count bottles, nationwide in the United States. A cGMP deviation detected N-nitroso-prazosin impurity C above acceptable limits. Consumers and healthcare providers should stop using this product immediately and contact Appco Pharma LLC or a healthcare provider for guidance.

Biocon Pharma
cGMP deviation:
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Health & Personal Care
HIGH
FDA DRUG

Biocon Prazosin Hydrochloride 2 mg Capsules Recalled for Nitrosamine Impurity (58,896 bottles, 2026)

Biocon Pharma Inc. recalled 58,896 bottles of Prazosin Hydrochloride Capsules, USP, 2 mg, 100-count bottle. The product was distributed nationwide in the USA and manufactured by Appco Pharma LLC. A cGMP deviation detected N-nitroso-prazosin impurity C above acceptable limits. Consumers and healthcare providers should stop using this product immediately and contact Appco Pharma LLC or their health‑

Prazosin Hydrochloride
cGMP deviation:
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Health & Personal Care
HIGH
FDA DRUG

Amneal TRAMADOL HYDROCHLORIDE 50 mg Recall 29,542 Bottles Over Impurity (2026)

Amneal Pharmaceuticals is recalling 29,542 bottles of TRAMADOL HYDROCHLORIDE tablets distributed nationwide in the United States. The recall cites a failed impurity specification for N-nitroso-desmethyl-tramadol (NDSRI) at the 24‑month stability interval. Consumers and healthcare providers should stop using the product immediately and contact Amneal for guidance.

TRAMADOL HYDROCHLORIDE
Failed Impurities/Degradation
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Health & Personal Care
MEDIUM
FDA DRUG

AvKARE Recalls Rosuvastatin Tablets Due to Dissolution Issues

AvKARE recalled 7,991 cartons of Rosuvastatin Tablets on December 31, 2025. The recall stems from the product being out of specification for dissolution. Consumers should stop using the medication immediately and consult healthcare providers for guidance.

MAGNESIUM SULFATE
Product mix
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Health & Personal Care
HIGH
FDA DRUG

Teva Octreotide Acetate Injectable Suspension Recall 21,930 Cartons Over Sterility Risk (2026)

Teva Pharmaceuticals recalled 21,930 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the United States. The recall stems from lack of assurance of sterility identified during an FDA inspection at the contract manufacturer. Healthcare providers and patients should stop using this product immediately and contact Teva or a physician for guidance.

OCTREOTIDE ACETATE
Lack of
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Recalled Tomum Minoxidil Hair Regrowth Treatment (Front view)
HIGH
CPSC

Tomum Minoxidil Hair Serum Recalled Over Child Poisoning Risk

Tomum recalled its Minoxidil Hair Growth Treatment on March 5, 2026, due to serious poisoning risks to children. The product lacks required child-resistant packaging, increasing the risk of ingestion. Consumers should stop using the product immediately and contact the company for a safe replacement.

Tomum Minoxidil Hair Serum Spray Bottles
The hair
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Health & Personal Care
HIGH
FDA DEVICE

Koven Technology BiDop 3 Pocket Doppler ES-100V3 Recalled for Fetal Labeling Issue (2026)

Koven Technology recalled 34 BiDop 3 Pocket Dopplers with BT2M20S8C fetal probes nationwide after regulators found the fetal indication on the labeling was not cleared under 510(k). The defect is labeling that misrepresents fetal use. Healthcare providers and patients should stop using the devices and follow recall instructions from the manufacturer.

Koven Technology
Product labeling
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Health & Personal Care
HIGH
FDA DRUG

K.C. Pharmaceuticals Sterile Eye Drops Recall 315,144 Bottles for Lack of Sterility (2026)

K.C. Pharmaceuticals recalled 315,144 sterile eye drop bottles distributed nationwide after lack of sterility. The products span several brands including GNP Eye Drops Redness and Dry Eye Relief, Leader Eye Drops Redness Relief, and Foster & Thrive Redness Relief Eye Drops. Consumers should stop using the products immediately and follow guidance from KC Pharmaceuticals or their healthcare provider

GNP Eye Drops Redness and Dry Eye Relief
Lack of
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Health & Personal Care
HIGH
FDA DRUG

ARTIFICIAL TEARS Dry Eye Relief Eye Drops Recalled in 2026 Over Sterility Concerns

More than 1.02 million bottles of Dry Eye Relief Eye Drops across multiple brands were recalled nationwide on March 3, 2026. The products were distributed by KC Pharmaceuticals and sold at retailers including Rite Aid, Meijer and H-E-B. The FDA notice cites a lack of assurance of sterility as the reason for the recall. Stop using these products immediately and contact KC Pharmaceuticals for next‑s

ARTIFICIAL TEARS
Lack of
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Health & Personal Care
HIGH
FDA DRUG

LEADER Ultra Lubricating Eye Drops Recalled for Sterility Issue (2026)

Cardinal Health distributed LEADER Ultra Lubricating Eye Drops and related store-brand lubricating eye drops nationwide. The recall cites a lack of assurance of sterility. Consumers should stop using these products immediately and contact KC Pharmaceuticals for guidance.

LEADER ULTRA LUBRICATING EYE DROPS
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Leader Artificial Tears Recalled 589,848 Bottles for Sterility Issue in 2026

Leader Artificial Tears Sterile Lubricant Eye Drops sold nationwide are recalled due to lack of assurance of sterility. The recall involves multiple store-brand lines distributed by Cardinal Health and others. Consumers should stop using the product immediately and follow recall guidance from KC Pharmaceuticals via email.

Leader
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD10C X-ray System Recall for 15 Units Worldwide (2026)

Philips Medical Systems Nederland B.V. recalled 15 Allura Xper FD10C radiography systems worldwide, including 7 in the United States and 8 overseas. The devices may fail to initiate X-ray imaging or intermittently stop imaging when using the wired foot switch. Facilities should stop using the devices and await recall instructions from Philips.

Philips Medical Systems Nederland B.V.
Philips has
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Tag Statistics

Total Recalls
1,035

Related Tags

poisoning riskimmediate actionstop use immediatelyfederal law violationcpsc regulatedadult productinfant productkitchenbathroomreplacement availablereturn for refundsuffocation risk