High Risk Recalls

Karison Foods Recalls Besan Ladoo Over Undeclared Milk Hazard

Product contains milk, which is undeclared in the ingredient statement.

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

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.

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.

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 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.

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 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.

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.

Alphatec Spine Recalls Lateral Navigation Disc Prep Instruments Due to Design Flaw

Due a design issue where the navigated array connection geometry is incorrect.

Alphatec Spine Recalls Surgical Instruments Over Connection Issue

Due a design issue where the navigated array connection geometry is incorrect.

Toyota Sienna Hybrid Recall 2025 Over Third-Row Seatback Bolts

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.

Cipla Lanreotide Acetate Injection Recall: 15,221 Syringes Over Particulate Matter (2026)

Kia Recalled 2025 Sorento Hybrid and 2024-2025 Sorento SUVs for BDC Software Issue

Alvogen Recalls Levothyroxine Sodium Tablets Due to Mix-Up

Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.

Wizcure Pharmaa Recalls Fluorescein Sodium Ophthalmic Strips Over Sterility Concerns

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.