Health & Personal Care Recalls

VANTIVE US HEALTHCARE Recalls Dialyzer Due to Dislodgement Hazard

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

VANTIVE US HEALTHCARE Recalls OXIRIS SET Dialyzer Over Dislodgement Risk

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

VANTIVE US Healthcare Recalls Dialyzer Due to Dislodgement Risk

VANTIVE US Healthcare recalled 264,040 Prismaflex ST150 Dialyzers on January 6, 2026. The devices pose a high risk of the deaeration chamber dislodging from the control unit. Healthcare providers and patients must stop using these devices immediately.

VANTIVE US Healthcare Recalls Dialyzer Over Dislodgement Risk

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

VANTIVE US Healthcare Recalls Dialyzer Over Dislodgement Risk

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

VANTIVE US Healthcare Recalls Dialyzer Over Dislodgement Risk

VANTIVE US Healthcare recalled 230,596 units of the PRIMSAFLEX M100 Set on January 6, 2026. The recall follows a risk of dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.

VANTIVE US HEALTHCARE Recalls Dialyzer Over Dislodgement Risk

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

VANTIVE US HEALTHCARE Recalls Dialyzer Due to Dislodgement Hazard

VANTIVE US HEALTHCARE recalled 87,436 Prismaflex ST100 Dialyzers on January 6, 2026. The recall follows reports of potential dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.

Straumann USA Recalls Impression Caps Over Mix-Up Hazard

The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.

Encon Safety Products Recalls AQ 120 GFEW Aquarion Preserved Cartridges in 2026

Medline Nail Kit Recalled Over Sterility Concerns

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Biomerieux Recalls VITEK 2 Antibiotic Susceptibility Cards Due to False Results

Biomerieux recalled 2,668,954 VITEK 2 Gram-negative susceptibility cards on January 5, 2026. The recall addresses potential false resistant results for certain antibiotic tests. Healthcare providers and patients must stop using the product immediately.

Medline Recalls Convenience Kits Over Sterility Concerns

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Encore Medical Recalls Knee Tibial Insert Due to Packaging Error

Encore Medical, LP recalled 19 units of the EMPOWR 3D Knee Tibial Insert on January 5, 2026. The recall follows the discovery of a packaging error that may cause surgical delays. Healthcare providers and patients should stop using the device immediately.

Raz Design Raz-AT Mobile Shower Commode Chair Recall for 66 Units Over Bracket Engagement Hazard (Z-

Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place.

Encore Medical Recalls EMPOWR Acetabular System Over Packaging Errors

Encore Medical, LP recalled 49 units of the EMPOWR Acetabular System on January 5, 2026. Packaging errors may cause surgical delays, potentially affecting patient safety. Healthcare providers should stop using these devices immediately.

Medline Recalls Saline Wound Wash Over Sterility Concerns

Medline Industries recalled 104,608 units of sterile saline wound wash on January 5, 2026. The product may not have met the required sterility assurance level. Consumers should stop using this product immediately and follow recall instructions.

Medline Recalls Wound Wash Kits Over Sterility Concerns

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline Recalls Sterile Saline Wound Wash Over Sterility Concerns

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

AVID Medical Recalls Transport Bag Kit Over Sterility Risk

AVID Medical recalled 1,500 units of the TRANSPORT BAG KIT on January 2, 2026. A seal issue with the Tyvek bag may compromise the sterility of the kit. The recall affects healthcare providers and patients in New Jersey.