poisoning risk Recalls

612 recalls tagged with “poisoning risk”.

Health & Personal Care
HIGH
FDA DRUG

Teva Octreotide Acetate Injectable Suspension Recall 19,869 Cartons Nationwide (2026)

Teva Pharmaceuticals USA recalled 19,869 cartons of Octreotide Acetate for Injectable Suspension nationwide in the United States after FDA inspection flagged lack of assurance of sterility at the contract manufacturer. The FDA cited quality system deficiencies at Pharmathen International S.A. in Greece. Healthcare providers and patients should stop using the product immediately and contact Teva or

OCTREOTIDE ACETATE
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Xanax XR Alprazolam Recall Over Failed Dissolution Specifications Affects US Nationwide Distribution

Xanax XR extended-release alprazolam recall issued March 17, 2026 remains active. Viatris Specialty LLC distributes the drug nationwide in the United States. The issue is failed dissolution specifications. Patients and healthcare providers should stop using the product immediately and follow the recall instructions for guidance.

XANAX
Failed Dissolution
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Health & Personal Care
HIGH
FDA DRUG

Cipla USA Lanreotide Injection Recall for Sterility Assurance Issue (2026)

Cipla USA Inc. recalls 54,583 Lanreotide acetate injections nationwide after FDA flagged sterility assurance concerns at a contract manufacturer. The recall covers a box containing one pre-filled syringe and one safety needle. Healthcare providers and patients should stop using the product immediately and follow the company’s guidance for disposal and refunds.

LANREOTIDE ACETATE
Lack of
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Food & Beverages
HIGH
FDA FOOD

Pure Vitamins and Natural Supplements Blue Bull Extreme Recall for undeclared sildenafil (High risk)

FDA analysis found undeclared sildenafil in Blue Bull Extreme Male Enhancement Supplement sold by Pure Vitamins and Natural Supplements. A total of 15 pouches per box were distributed. The product’s UPC is 707443349917 and it is linked to New Jersey. Consumers should stop use immediately and seek refund or replacement.

Pure Vitamins and Natural Supplements
FDA analysis
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Recalled Kluster Fun Tabletop Magnet Chess Game (Sold in White Pouch)
HIGH
CPSC

Stoney Games Recalls Kluster Magnet Chess Games Over Ingestion Risk

Stoney Games recalled Kluster Fun Tabletop Magnet Chess Games on March 12, 2026, due to a serious ingestion hazard. The games contain loose, high-powered magnets that can be swallowed by children, posing a risk of severe injury or death. Consumers should immediately stop using the games and contact Stoney Games for replacement options.

Stoney Games
The recalled
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Food & Beverages
HIGH
FDA FOOD

Lone Star Dairy Products Recalls 1.79M Lbs Spray Dried Dairy Powder Over Salmonella Risk (2026)

Lone Star Dairy Products LLC issued an active recall of 1.79 million pounds of spray dried dairy powder sold in the United States after Salmonella spp. was identified in finished product testing. The affected product is packaged in 25 kg bags or 1 metric ton totes. Consumers should not consume the product and should contact Lone Star Dairy Products LLC for refund or replacement information via e‑m

Lone Star Dairy Products
Salmonella spp.
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Saline Solution Recalled for Lack of Sterility Assurance (2026)

Fresenius Kabi USA recalled saline injections distributed nationwide, including Alaska and Puerto Rico. The action covers multiple batch numbers with sterility concerns. Healthcare providers and patients should stop using the product immediately and follow official guidance for replacement options.

SODIUM CHLORIDE
Lack of
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Health & Personal Care
HIGH
FDA DRUG

BD and Fresenius Kabi Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)

BD Becton, Dickinson and Company and Fresenius Kabi USA recall 0.9% Sodium Chloride Injection, USP, 250 mL in a single-dose bag nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers and patients should stop using the product immediately and follow guidance from Fresenius Kabi or their provider.

SODIUM CHLORIDE
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Zydus Icosapent Ethyl Capsules Recalled for Oxidized Ingredient in 60,541 Bottles (2026)

Zydus Pharmaceuticals USA Inc. is recalling 60,541 bottles of Icosapent Ethyl Capsules, 1 g, 120 capsules per bottle, distributed nationwide in the United States. The recall cites oxidized Icosapent Ethyl causing red dots inside capsules and melted capsules. Patients should stop using the medicine immediately and contact Zydus Pharmaceuticals USA Inc. or their clinician for guidance.

ICOSAPENT ETHYL
Failed Tablet/Capsule
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Food & Beverages
HIGH
FDA FOOD

JFE Franchising Dumpling Party Tray Recall for Glass Contamination (2026)

JFE Franchising Inc. recalls Dumpling Party Tray products and a Cheetos Flamin Hot Loaded Dumpling item after glass fragments were found in the trays. The FDA enforcement report lists glass as the foreign object hazard. Consumers should not eat these products and should seek refunds or replacements via email.

JFE Franchising
Foreign Object
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Health & Personal Care
HIGH
FDA DEVICE

Cook Medical Thal-Quick Chest Tube Tray Recalled for Expiration Dates Exceeding Shelf Life

Cook Medical recalled the Thal-Quick Chest Tube Tray, reference part number C-TQTSY-3200, Order G07242, due to expiration dates that exceed true shelf life. The recall is active and worldwide. The hazard is labeling that misstates shelf life. Patients and healthcare providers should stop using the affected devices immediately and follow Cook’s recall instructions.

Cook
Products from
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Health & Personal Care
HIGH
FDA DEVICE

Cook Medical Approach CTO-12 Micro Wire Guide Recall Affects 49 Units for Expired Shelf-Life Labels

Cook Medical recalled 49 units of the Approach CTO-12 Micro Wire Guide due to expiration dates that exceed the true shelf life. The recall covers two reference part numbers and multiple lots distributed worldwide. Healthcare providers and patients should stop using the affected devices immediately. Follow the manufacturer’s recall instructions or contact a healthcare provider for guidance.

Cook
Products from
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