chemical hazard Recalls

1,035 recalls tagged with “chemical hazard”.

Food & Beverages
HIGH
FDA FOOD

Taylor Farms Salad Kit Recalled Due to Undeclared Allergens

Taylor Farms recalled 8,284 units of its Honey Balsamic Salad Kit on August 21, 2025. The recall stems from undeclared allergens including sesame and soy. Consumers should not consume the affected products and seek refunds or replacements.

Taylor Farms Retail
Undeclared allergens
Read more
Food & Beverages
HIGH
FDA FOOD

Latitude 36 Foods Issues Recall of Honey Balsamic Dressing

Latitude 36 Foods recalled 46,800 units of Honey Balsamic dressing on August 21, 2025. The dressing contains undeclared soy and sesame, posing a serious health risk. Consumers should not consume the product and seek a refund.

Latitude 36 Foods
Product contains
Read more
Health & Personal Care
HIGH
FDA DEVICE

Abbott Point Of Care Recalls i-STAT CG8+ Cartridge Over Clearance Issues

Abbott Point Of Care recalled 8,962,450 i-STAT CG8+ cartridges on August 21, 2025. The recall affects cartridges lacking proper 510(k) premarket clearance for updated sample types. Patients and healthcare providers must stop using these devices immediately.

Abbott Point Of Care
Lack of
Read more
Food & Beverages
HIGH
FDA FOOD

Itacate Foods Recalls Chilaquiles Over Undeclared Dyes

Itacate Foods recalled 566 packages of CHARGE-UP CHILAQUILES on August 20, 2025. The product contains undeclared Yellow #5 and Yellow #6, posing a health risk. Consumers should not consume the product and seek a refund or replacement.

Itacate Foods
Undeclared Yellow
Read more
Food & Beverages
HIGH
FDA FOOD

Hostess Recalls Ding Dongs Due to Mold Contamination

Hostess recalled 60,630 cases of Ding Dongs on August 20, 2025, following reports of mold contamination. The recall affects various packaging sizes sold across multiple states. Consumers should not consume the product and seek refunds or replacements immediately.

The J.M. Smucker
Mold. The
Read more
Health & Personal Care
HIGH
FDA DRUG

Major Pharmaceuticals Recalls Carvedilol Tablets Over Impurity Hazard

Major Pharmaceuticals recalled 26,628 cartons of Carvedilol Tablets on August 20, 2025. The recall stems from N-Nitroso Carvedilol Impurity-1 levels exceeding FDA limits. Consumers should stop using the product immediately and consult their healthcare provider.

Major Pharmaceuticals
CGMP Deviations:
Read more
Food & Beverages
HIGH
FDA FOOD

Itacate Foods Recalls Lentil Soup Over Undeclared Dyes

Itacate Foods recalled 154 packages of CAMPSITE LENTEJAS lentil soup on August 20, 2025. The recall follows the discovery of undeclared Yellow #5 and Yellow #6, which can cause allergic reactions. Consumers should stop using the product immediately.

Itacate Foods
Undeclared Yellow
Read more
Health & Personal Care
HIGH
FDA DRUG

Baxter Healthcare Recalls Acetaminophen Injection Over Discoloration Risk

Baxter Healthcare Corporation recalled 13,000 containers of Acetaminophen Injection on August 20, 2025. The recall follows reports of discoloration that may affect product safety. Consumers should stop using the medication immediately and contact their healthcare providers for guidance.

Baxter Healthcare Corporation
Discoloration
Read more
Food & Beverages
HIGH
FDA FOOD

Toto Foods Recalls S'Mores Cookies Over Soy Allergy Risk

Toto Foods recalled 120,180 units of S'Mores Ooey Gooey Cookies on August 20, 2025. The product label conflicts regarding soy content pose a health risk to consumers with soy allergies. The cookies were distributed across 13 states including California and New York.

Toto Foods
Product label
Read more
Food & Beverages
HIGH
FDA FOOD

Frozen Cooked Shrimp Recalled Due to Cesium-137 Contamination

Best Yet, Arctic Shores, and Great American branded frozen cooked shrimp were recalled on August 19, 2025, due to potential contamination with Cesium-137. The recall affects 11,081 cases distributed across nine states including California and Virginia. Consumers should stop using these products immediately and contact the manufacturer for refunds.

Best Yet
Product manufactured
Read more
Health & Personal Care
HIGH
FDA DRUG

Medline Recalls Povidone-Iodine Solution Due to Potency Issues

Medline Industries recalled 2,680 bottles of Povidone-Iodine 10% Solution on August 19, 2025. The product is subpotent, posing a risk to users. Consumers should stop use immediately and contact their healthcare provider.

POVIDONE-IODINE
Subpotent drug
Read more
Health & Personal Care
HIGH
FDA DRUG

Amneal Pharmaceuticals Recalls Chlorpromazine Tablets Over Contamination Risk

Amneal Pharmaceuticals recalled 13,130 bottles of Chlorpromazine Hydrochloride Tablets on August 18, 2025, due to contamination concerns. The recall affects specific lots identified by their lot numbers AM240147, AM240148, AM240664, and AM240665. Consumers should stop using the tablets immediately and contact their healthcare provider for further guidance.

Chlorpromazine Hydrochloride
Presence of
Read more
Health & Personal Care
HIGH
FDA DRUG

Amneal Pharmaceuticals Recalls Sulfamethoxazole Tablets Over Hazard

Amneal Pharmaceuticals recalled over 133,000 bottles of Sulfamethoxazole and Trimethoprim Tablets on August 18, 2025. The recall stems from the detection of a microorganism in the packaging material, raising health concerns. No microorganisms were found on the tablets themselves.

SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
Read more
Health & Personal Care
HIGH
FDA DRUG

Amneal Pharmaceuticals Recalls Chlorpromazine Hydrochloride Tablets

Amneal Pharmaceuticals recalled 3,363 bottles of Chlorpromazine Hydrochloride Tablets on August 18, 2025. The recall stems from the presence of a microorganism in packaging material. No microorganisms were detected in the tablets themselves, but consumers should stop using the product immediately.

Chlorpromazine Hydrochloride
Presence of
Read more