Health & Personal Care
HIGH
FDA DEVICE
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
Due a
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DRUG
Cipla Lanreotide Acetate Injection Recall: 15,221 Syringes Over Particulate Matter (2026)
LANREOTIDE ACETATE
Presence of
Vehicles & Parts
HIGH
Vehicles & Parts
HIGH
Health & Personal Care
HIGH
FDA DRUG
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.
LEVOTHYROXINE SODIUM
Product Mix-Up:
Health & Personal Care
HIGH
FDA DRUG
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.
C20H10NA2O5 FLUORESCEIN SODIUM OPHTHALMIC STRIPS
Lack of
Health & Personal Care
HIGH
FDA DRUG
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.
VISTA GONIO EYE LUBRICANT
Lack of
Health & Personal Care
HIGH
FDA DRUG
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.
Wizcure Pharmaa Private
Lack of
Health & Personal Care
HIGH
FDA DEVICE
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.
Miach Orthopaedics
Incorrect expiration
Health & Personal Care
HIGH
FDA DEVICE
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.
Medica
A systematic
Health & Personal Care
HIGH
FDA DRUG
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 Private
Lack of
Health & Personal Care
HIGH
FDA DRUG
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.
Wizcure Pharmaa Private
Lack of
Health & Personal Care
HIGH
FDA DRUG
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.
VISTA MEIBO TEARS PROPYLENE GLYCOL 0.6% W/V ADVANCED DRY EYE RELIEF LUBRICATING DROPS 10 ML
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Medline Industries Recalls IV Administration Sets Due to Leakage Risk
Medline Industries, LP
Under circumstances
Food & Beverages
HIGH
FDA FOOD
WFM Purchasing Recalls Brussel Sprouts & Kale Slaw Over Allergen Risk
WFM Purchasing, LP recalled 88 units of Brussel Sprouts & Kale Slaw on December 31, 2025. The product contains undeclared fish and egg allergens, posing a serious health risk. Consumers in New York, New Jersey, and Virginia should not consume this product.
WFM Purchasing, LP
Undeclared Fish
Health & Personal Care
HIGH
FDA DEVICE
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.
Centinel Spine
Products were
Health & Personal Care
HIGH
FDA DRUG
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.
VISTA HYPROMELLOSE DRY EYE RELIEF
Lack of
Health & Personal Care
HIGH
FDA DEVICE
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.
Intuitive Surgical
Robotic-assisted surgical
Health & Personal Care
HIGH
FDA DRUG
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.
ONDANSETRON
Defective container:
Health & Personal Care
HIGH
FDA DRUG
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.
Fluocinolone Acetonide
Failed Impurities/Degradation