95,064 total recalls in our database
Takeda Development Center Americas
Defective Delivery System: tablets may be missing, in whole or in part, the laser drilled holes on the metformin core of the Actoplus met XR tablets.
Subpotent Drug: One lot of product does not meet the product specification for Assay test at 3 month long term stability condition.
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Jubilant Cadista Pharmaceuticals
Discoloration: Presence of dark discoloration or brown spots on the edges of the tablets.
CGMP Deviations; rejected product was used to manufacture final bulk lot
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Correct Labeled Product Mispack: confirmed report involving a single unit of properly labeled Heparin in 0.45% Sodium Chloride for Injection (NDC 0409-7651-03, Lot 87903FW) that was found inside a case of Magnesium Sulfate in Water for Injection.
Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name on the packaging component that may cause confusion.
CooperSurgical
The seal of the sterile pouch may be compromised, thereby increasing the risk of infection.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Orthosensor
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements per product specification for biological residues determined by LAL testing.
The reason for this field action is due to the mounting of a non-tamper-resistant (ordinary) battery drawer on some BABY440 hearing aids. The correct battery drawer is tamper-resistant and require a special tool to open it.
Orthosensor
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Firm received sporadic reports of discoloration on certain lots of the product, which has been identified as common mold.
The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.
When multiple CARESCAPEMonitor B450 or B850 units are connected to the same network and a network overload occurs for a prolonged time, the monitors may simultaneously restart as designed. The monitor restart will not be completed until the network issue has been corrected.
Potential for the tethered plug on the hub of the NeoMed Enteral Feeding Tubes with Enteral Only Connectors to inadvertently open after closure.
Product marketed in U.S. does not have sufficient data to ensure that it will meet the internal burst pressure specifications at the end of 5 yrs shelf-life