We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.
Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Magellan recalls LeadCare Plus Blood Lead Test Kit (Catalog 82-0004) due to false positive lead results from third-party micro-collection devices, causing unnecessary testing. All units affected.
AVID Medical recalls Halyard CARDIAC CATH TRAY SHANDS JAX kits (models SHND401-04 and SHND401-05) due to potential risk of medline syringe rotating adaptor unwinding, which may cause loose or full disconnection between syringe and manifold.
Cipla USA recalls Lanreotide injection due to potential lack of sterility in manufacturing. Products with specific NDC numbers and expiration dates are affected. Consumers should check their product details and contact Cipla for guidance.
Endo USA recalls 5x1mL Buprenorphine injections due to crystallization risk. Affected lots expire 02/2027 and 03/2027. Contact for return instructions.
Cipla USA recalls Lanreotide Injection 120 mg/0.5 mL syringes due to potential contamination from inadequate visual inspection at manufacturing. This could lead to infections if used.
