Health & Personal Care Recalls

Alphatec Spine Recalls Surgical Instruments Over Connection Issue

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

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

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

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

Medica Recalls Capillary Tube Kit Over False Potassium Readings

Medica recalled 1,578 units of its Capillary Tubes on December 31, 2025. A systematic positive bias of up to 20% can produce false elevation results in patient potassium levels. Healthcare providers and patients must stop using the device immediately.

Wizcure Pharmaa Recalls Eye Drops Due to Sterility Concerns

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.

Wizcure Pharmaa Recalls Vista Gel Eye Drops Due to Sterility Issues

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

Wizcure Pharmaa Recalls Eye Drops Due to Sterility Risk

Wizcure Pharmaa PVT. LTD. recalled 11,520 cartons of Vista Meibo Tears Eye Drops on December 31, 2025. The recall occurred due to lack of assurance of sterility, posing a high risk to consumers. The affected product was distributed nationwide in the USA.

Medline Industries Recalls IV Administration Sets Due to Leakage Risk

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.

Wizcure Pharmaa Recalls Vista Gonio Eye Lubricant Over Sterility Issues

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

Wizcure Pharmaa Recalls Ophthalmic Strips Over Sterility Concerns

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

BioGlo Ophthalmic Strips Recalled Over Sterility Concerns

BioGlo Fluorescein Sodium Ophthalmic Strips are recalled due to sterility issues. The recall affects 184,320 containers distributed nationwide in the USA. Consumers should stop using the product immediately.

Centinel Spine Recalls Prodisc C SK Cervical Disc Over Mislabeled Product

Centinel Spine recalled 20 units of the Prodisc C SK cervical disc on December 31, 2025. The products were mislabeled as the 6mm variant but included the 5mm variant. The recall affects patients in multiple states including California and New York.

Miach Orthopaedics Recalls BEAR Implant Over Expiration Date Error

Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will also be incorrect.

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.

Zydus Pharmaceuticals Recalls Icosapent Ethyl Capsules Over Subpotency

Subpotent Drug: Due oxidation caused by leakage of the contents of the Icosapent Ethyl 1g capsules. Use of the affected product may lead to inconsistent therapeutic effects and an increase in potential gastrointestinal side effects in some patients.

Glenmark Pharmaceuticals Recalls Ondansetron Tablets Over Packaging Issues

Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.

Sun Pharmaceutical Fluocinolone Acetonide Topical Solution Recall 24,624 Bottles (2025)

Failed Impurities/Degradation Specifications: Out of specification result was obtained for the known impurity D.

Intuitive Surgical Recalls da Vinci 5 Display Over High Injury Risk

Intuitive Surgical recalled 47 da Vinci 5 Surgeon Console Viewer Displays on December 30, 2025. The devices may lose display functionality, risking surgical injury. Healthcare providers should stop using the consoles immediately and follow recall instructions.

Siemens Recalls Interventional Fluoroscopic X-Ray System Over Imaging Risk

Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.