Health & Personal Care Recalls

Medline Recalls Urology Kits Over Leak and Vapor Risks

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 Recalls Medical Kits Due to Suction Irrigator Leak Hazard

Medline Recalls Medical Kits Over High Burn Risk

Alembic Pharmaceuticals Recalls Fesoterodine Tablets for Impurity Risk

Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.

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 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.

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.

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 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 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 Recalls Vitrectomy Lenses Due to Infection Risk

Vortex Surgical recalled 14,789 single-use vitrectomy lenses on December 16, 2025. The recall affects models with potential seal voids that could lead to bioburden contamination. Patients and healthcare providers must stop using these devices 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 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 IOL Marker Recalled 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 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.

SunMed Recalls Broselow Pediatric Emergency Tape Over Dosing Errors

Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.

Philips Medical Systems Issues Recall for Allura Xper FD10/10

Broselow Pediatric Emergency Tape Recalled Over Dosing Errors

Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.