1,732 product recalls found in this category. Browse through all safety alerts and stay informed.
High Activity Category
This category has a significant number of recalls. Please check regularly for updates.
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 recalled 2,724 OXIRIS SET dialyzers on January 6, 2026. The recall follows reports of potential dislodgement of the deaeration chamber from the Prismaflex Control Unit. Patients and healthcare providers must stop using the device immediately.
VANTIVE US Healthcare recalled 93,576 Prismaflex HF1000 Sets on January 6, 2026. The recall addresses a potential dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately and follow provided instructions.
Straumann USA recalled 561 units of its Impression Post Closed Tray on January 6, 2026. The recall occurred due to a mix-up where impression caps were mistakenly packaged in magenta instead of the intended brown. Healthcare providers and patients must stop using the device immediately.
Encon Safety Products recalls AQ 120 GFEW Aquarion Preserved Cartridges sold nationwide through multiple retailers. The recall cites cGMP deviations in manufacturing. Stop using the product immediately and follow recall guidance from Encon Safety or your healthcare provider.
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, 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.
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 Industries has recalled 3,578,805 units of its sterile saline wound wash due to potential sterility assurance issues. The recall, effective January 5, 2026, affects products distributed worldwide, including in the U.S. Consumers should stop using the product immediately.
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 Industries recalled 8,773 units of its Nail Kit, Model Number DYKM1528, on January 5, 2026. The recall stems from a failure to meet required sterility assurance levels in the saline wound wash. Patients and healthcare providers should stop using the product immediately.
Medline Industries recalled 10,550 wound care kits on January 5, 2026, due to potential sterility issues. The recall affects several model numbers, including DYKM1361A and DYKM2013. Consumers should stop using the kits immediately and follow the manufacturer's instructions.
Medline Industries recalled 1,640 units of its Nail Kit, Model POD14214, on January 5, 2026. The recall stems from concerns that the sterile saline wound wash may not meet required sterility standards. Patients and healthcare providers must stop using the product immediately.
Alphatec Spine recalled 15 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The navigated array connection geometry is incorrect, posing risks during surgical procedures. Healthcare providers and patients should stop using the instruments immediately.
Alphatec Spine recalled 7 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The incorrect navigated array connection geometry poses a high hazard risk in surgical settings. Healthcare providers and patients must stop using the devices immediately.
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 USA, Inc. is recalling 15,221 Lanreotide Acetate Injection syringes nationwide in the United States after detecting particulate matter. The defect is the presence of particulate matter in the injectable solution. Healthcare providers and patients should stop using the product immediately and contact Cipla USA for guidance.
Alvogen, Inc. recalled Levothyroxine Sodium Tablets on January 21, 2026, after a pharmacy reported a mix-up with dosages. Some bottles contained 88 mcg tablets instead of the prescribed 150 mcg. The recall affects 1,000 tablets from lot # MHA21825, with an expiration date of December 31, 2027.
Wizcure Pharmaa recalled 10,080 boxes of Fluorescein Sodium Ophthalmic Strips on December 31, 2025, due to sterility issues. The recall affects products packaged in 100-count and 300-count boxes. Consumers should stop using these products immediately and consult healthcare providers for guidance.
Wizcure Pharmaa recalled 5,760 cartons of Vista Tears Eye Drops on December 31, 2025. The recall follows a lack of assurance of sterility in the product. Consumers should stop using the drops immediately and contact a healthcare provider for guidance.