immediate action Recalls

Medline Recalls Medical Procedure Kits Due to Leakage Risk

Vortex Surgical Recalls 23G and 25G Laser Probes Due to Infection Risk

Vortex Surgical recalled 14,789 laser probes on December 16, 2025, due to potential contamination risks. The recall affects devices distributed worldwide, including 8,651 units in the U.S. Consumers should stop using these devices immediately.

Vortex Surgical Recalls Forceps and Cannula Due to Infection Risk

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

Medline Recalls Medical Kits Over High Burn Risk

Medline Recalls Medical Kits Due to Suction Irrigator Leak Hazard

Medline Medical Kits Recalled Over Strykeflow 2 Suction Hazard

Medline recalled 4,536 medical procedure kits on December 16, 2025. The kits contain Stryker's Strykeflow 2 Suction Irrigators that may leak and emit vaporized saline. The recall affects various models used in surgeries nationwide.

Medline Medical Kits Recalled Due to Suction Irrigator Hazards

Medline recalled 41,432 medical procedure convenience kits on December 16, 2025. The kits contain Stryker's Strykeflow 2 Suction Irrigators that may leak or emit vaporized saline. This defect poses a high risk of injury during medical procedures.

Vortex Surgical Recalls Disposable Elevator Over Infection Risk

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

Vortex Surgical Recalls Convenience Kits Over Infection Risk

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

Vortex Surgical Injection Kit Recalled Over Infection Risk

Vortex Surgical recalled 14,789 I2 Injection Kits on December 16, 2025. Voids in the seal of Tyvek pouches may compromise sterility, posing an infection risk. Healthcare providers and patients must stop using this device immediately.

Vortex Surgical Recalls 25GA Backflush Pouches Over Infection Risk

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

ASK Foods Recalls Publix Rice & Pigeon Peas Over Undeclared Soy Allergen

ASK Foods recalled 2,078 units of Publix Rice & Pigeon Peas on December 16, 2025. The recall stems from an undeclared soy allergen. This poses a serious risk to consumers with soy allergies.

Medline Recalls Urology Kits Over Leak and Vapor Risks

SpecGx Recalls Oxycodone and Acetaminophen Tablets Over Missing Imprint

Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.

Vortex Surgical Polisher Recalled Due to Infection Risk

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

Vortex Surgical Recalls Injection Cannula Due to Infection Risk

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

Qunol Turmeric Capsules Recalled Due to Mold Contamination

Qunol recalled Extra Strength Turmeric Capsules due to mold contamination in raw materials. The recall affects over 3,000 units distributed across 27 states. Consumers should stop use and seek refunds immediately.

Vortex Surgical Recalls Internal Delivery Device Over Infection Risk

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

Vortex Surgical Recalls Illuminated Depressor Due to High Hazard

SpecGx Recalls Oxycodone and Acetaminophen Tablets Due to Missing Imprint

Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.