Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 13–24 of 105 recalls
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Due to packaging discrepancy with incorrect product size mixed up.
Due to packaging discrepancy with incorrect product size mixed up.
A product error defect may cause incorrect bracket placement.
A single lot of expired syringes were distributed due to a distribution system control failure.
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.
Surgical light assembly may not adequate support the weight of the ceiling cover.
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.