immediate action Recalls

Sevillo Fine Foods Recalls 2,372 Units of Slow Roasted Diced Tomatoes (2026 Recall)

Product may contain foreign material (metal fragments).

Organic Spices Recalls Celery Salt Over Mislabeled Ingredient

Organic Spices recalled 4,692 jars of celery salt on January 14, 2026. The product is mislabeled and contains salt, posing a risk to consumers. The recall affects multiple states including California and Texas.

KVK-Tech Inc. Recalls Oxycodone Hydrochloride Tablets Over Seal Defects

KVK-Tech Inc. recalled 31,676 packages of Oxycodone Hydrochloride Tablets on January 14, 2026. Defective seals may cause tablets to fall out, posing a health risk. Customers should stop using the product immediately and seek guidance from healthcare providers.

Organic Spices Recalls Garlic Salt Due to Mislabeled Product

Organic Spices, Inc. recalled 6,288 jars of garlic salt on January 14, 2026. The product contains salt, which is not listed on the label. The recall impacts several states including California and New York.

Organic Spices Recalls Sumac Due to Mislabeled Salt Content

Organic Spices Inc recalled 980 cases of organic sumac on January 14, 2026. The product contains mislabeled salt, posing a health risk to consumers. The recall affects 11,760 jars distributed across multiple states in the U.S.

Edermy Recalls Medical Devices Due to Lack of 510K Clearance

Edermy Recalls PIE Trolley System Due to Lack of 510K Clearance

MG Foods Recalls Breakfast Burrito Due to Plastic Fragments

foreign material (small hard plastic fragments)

Laerdal Medical Recalls Suction Units Over Electromagnetic Noise Hazard

Laerdal Medical recalled 1,202 Compact Suction Units on January 13, 2026. The recall affects models LCSU 4, 800 ml and LCSU 4, 300 ml due to excessive electromagnetic noise. Patients and healthcare providers must stop using the devices immediately.

Baxter Infusion Pump Recalled Due to Incomplete Testing

Baxter Healthcare recalled five infusion pumps on January 13, 2026. The pumps were released without full testing, including critical occlusion alarm checks. Healthcare providers and patients must stop using the device immediately.

Medtronic Recalls Octopus Nuvo Tissue Stabilizer Due to Assembly Issue

During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

McCain Foods Recalls Ore-Ida Tater Tots Due to Plastic Fragments

Foreign material (small hard plastic fragments).

Waldemar Link Endo-Model Replacement Plateau Recall for Detachment Risk (2026)

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Waldemar Link Endo-Model Replacement Plateau Recalled for 7 Units Worldwide (2026)

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Waldemar Link Recalled 3 Endo-Model Replacement Plateau Implants (2026)

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Waldemar Link Endo-Model Replacement Plateau Recalled for Detachment Risk

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Waldemar Link SL Connection Component Recall Due to Fracture Risk

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Waldemar Link Endo-Model Replacement Plateau Recall for 3 Units Worldwide (2026)

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Teva Isotretinoin 40 mg Capsules Recalled for Superpotent and Subpotent Lots (D-0446-2026)

Teva Pharmaceuticals USA, Inc. recalls 8,376 isotretinoin 40 mg capsules distributed to FL, OH, PR and MS after FDA enforcement report flags superpotent and subpotent lots. Patients should stop use and contact their healthcare providers for guidance.

Teva Isotretinoin 30 mg Recall Active for Potency Variations in 10-Count Packs

Teva Pharmaceuticals USA, Inc. recalls 21,984 packages of Isotretinoin Capsules, USP, 30 mg. The lots are distributed to Florida, Ohio, Puerto Rico and Mississippi. The recall is active as of April 15, 2026.