chemical hazard Recalls

1,035 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DRUG

Novadoz Pharmaceuticals Recalls Glycopyrrolate Oral Solution Over Safety Concerns

Novadoz Pharmaceuticals LLC recalled Glycopyrrolate Oral Solution on December 15, 2025, due to failed impurities and degradation specifications. The recall affects Rx only products manufactured by MSN Pharmaceuticals Inc. Consumers should stop using this medication immediately.

GLYCOPYRROLATE
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DEVICE

Broselow Recall Due to Dangerous Dosing Errors in ALS Organizer

Broselow recalled 384 units of their Domestic Complete ALS Organizer on December 15, 2025, due to harmful dosing errors. The recalled product affects dosages for Vecuronium, Flumazenil, and Ketamine. Healthcare providers and patients must stop using the device immediately.

SunMed Holdings
Product contains
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Food & Beverages
HIGH
FDA FOOD

So Delicious Dairy Free Frozen Dessert Recalled Due to Foreign Material

So Delicious Dairy Free recalled 4,665,608 units of its Salted Caramel Cluster Cashewmilk frozen dessert on December 15, 2025. The recall follows the discovery of foreign material in the product. Consumers should not consume this item and seek a refund or replacement immediately.

WhiteWave - Louisville Pilot Plant
Foreign material
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Health & Personal Care
HIGH
FDA DEVICE

Broselow Pediatric Emergency Tape Recalled Over Dosing Errors

SunMed Holdings recalled 20,583 units of Broselow Pediatric Emergency Rainbow Tape on December 15, 2025. The product contains harmful dosing errors for critical medications including Vecuronium, Flumazenil, and Ketamine. Healthcare providers and patients must stop using the tape immediately and follow recall instructions.

SunMed Holdings
Product contains
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Health & Personal Care
HIGH
FDA DEVICE

Broselow Recall: Harmful Dosing Errors in Pediatric Organizer

Broselow recalled 89 units of the BROSELOW FILLED BROSELOW ORGANIZER on December 15, 2025. The product contains harmful dosing errors for critical medications. Healthcare providers must stop using the device immediately.

SunMed Holdings
Product contains
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Health & Personal Care
HIGH
FDA DEVICE

Diagnostica Stago Recalls Asserachrom HPIA Kit Over False Negatives

Diagnostica Stago issued a recall for 438 Asserachrom HPIA kits on December 15, 2025. The kits, used to detect PF4 antibodies, may produce false negative results. The affected lot is 271288, distributed worldwide including multiple U.S. states.

Diagnostica Stago
Potential for
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Food & Beverages
HIGH
FDA FOOD

D. Coluccio & Sons Recalls Amaretti Cookies Over Poison Risk

D. Coluccio & Sons recalled 800 units of Sapori Amaretti Almonds cookies on December 14, 2025, due to elevated hydrocyanic acid levels. The cookies were distributed in New York, New Jersey, Georgia, and California.

D. Coluccio & Sons
Contains elevated
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Food & Beverages
HIGH
FDA FOOD

Prima Vera Nueva Tamales Recalled Due to Listeria Risk

Prima Vera Nueva recalled 27,964 packages of BBQ Chipotle Bean & White Cheddar Tamales on December 12, 2025. The recall affects products due to potential contamination with Listeria monocytogenes. Consumers should not eat the tamales and seek a refund or replacement.

Prima Vera Nueva
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Prima Vera Nueva Recalls Butternut Squash Tamales for Listeria Risk

Prima Vera Nueva recalled 18,876 packages of Butternut Squash Tamales on December 12, 2025, due to potential contamination with Listeria monocytogenes. The recall affects products distributed in California and Nevada. Consumers should not consume the tamales and seek refunds or replacements.

Prima Vera Nueva
Potential contamination
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Kits Recalled Due to Cracked Tubing Hazard

Medline Industries, LP recalled 857 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive which can cause butyrate tubing to crack during use. Healthcare providers and patients must stop using these kits immediately.

Medline Industries, LP
Medline kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Kits Recalled Over Hazardous Adhesive

Medline Industries recalled 236 medical procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive that may cause butyrate tubing to crack. Patients and healthcare providers should stop using these kits immediately.

Medline Industries, LP
Medline kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Kits Recalled Due to Liquid Adhesive Hazard

Medline Industries, LP recalled 1,928 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive linked to cracking tubing during use. Healthcare providers and patients must stop using these kits immediately.

Medline Industries, LP
Medline kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Convenience Kits Recalled Over Adhesive Hazard

Medline Industries recalled select medical procedure convenience kits on December 12, 2025. The recall affects 40 units due to risks associated with MASTISOL liquid adhesive. The adhesive's tubing may crack during use, posing safety concerns.

Medline Industries, LP
Medline kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Medical Kits Over Adhesive Tubing Hazard

Medline Industries recalled 1,928 medical procedure kits due to a safety hazard involving butyrate tubing. The recall affects multiple kit models containing MASTISOL liquid adhesive. The defective tubing may crack during use, posing a risk to patients and healthcare providers.

Medline Industries, LP
Medline kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Kits Recalled Over Adhesive Tubing Risk

Medline Industries recalled 1,928 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive, which has defective butyrate tubing. Cracking during use poses a high risk to patients and healthcare providers.

Medline Industries, LP
Medline kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Procedure Kits Recalled Due to Tubing Hazard

Medline recalled 96 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective tubing that can crack during use. Patients and healthcare providers should stop using these products immediately.

Medline Industries, LP
Medline kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Kits Recalled Due to Hazardous Adhesive

Medline Industries recalled 1,928 medical procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective butyrate tubing. Patients and healthcare providers must stop using these kits immediately.

Medline Industries, LP
Medline kits
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Medical Kits Due to Adhesive Tubing Hazard

Medline Industries recalled 117 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective tubing that may crack. Stop using these kits immediately and follow manufacturer instructions for return.

Medline Industries, LP
Medline kits
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