Glycopyrrolate 0.2 mg/ml, 5 mL pre-filled syringe, Rx Only. Pharmakon Pharmaceuticals, Inc., 14450 Getz Rd., Noblesville, IN 46060, NDC#: 45183-0965-70.
Pharmakon Pharmaceuticals
Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
95,114 total recalls in our database
Pharmakon Pharmaceuticals
Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Failed Dissolution Specifications and Failed Tablet Specifications: High 30 minute dissolution test and presence of broken lozenges.
Central Admixture Pharmacy Services
Non Sterility; microbial contamination identified as Aspergillus species
Pharmakon Pharmaceuticals
Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Central Admixture Pharmacy Services
Non Sterility; microbial contamination identified as Aspergillus species
Central Admixture Pharmacy Services
Non Sterility; microbial contamination identified as Aspergillus species
Abrams Royal Pharamacy
Non-Sterility; analytical results found product to contain Sphingomonas paucimobilis
Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Pharmakon Pharmaceuticals
Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Customer complaints for failure to deliver the dose.
Central Admixture Pharmacy Services
Non Sterility; microbial contamination identified as Aspergillus species
Abrams Royal Pharamacy
Lack of Assurance of Sterility
Mylan Pharmaceuticals
Failed Impurities/Degradation Specifications: High out-of-specification results for a related compound obtained during routine stability testing.
Zimmer is recalling sterile-packaged implants and instruments packaged in six different package configurations due to packaging design verification test failures. Specifically, multiple test samples from each of the six configurations failed simulated distribution and shipping testing when the devices either breached inner or outer package trays or seal integrity was lost.
Becton Dickinson & Company
BD has initiated the recall of its Vacutainer CPT Cell Preparation Tube due to poor separation, resulting in a reduced number of recovered mononuclear cells.
Smiths Medical ASD
The tube fastener on the ET Tube Holder may compress the tracheal tube when used which may cause difficulty when locking the ET Tube Holder in place or difficulty when passing a suction catheter.
Zimmer is recalling sterile-packaged implants and instruments packaged in six different package configurations due to packaging design verification test failures. Specifically, multiple test samples from each of the six configurations failed simulated distribution and shipping testing when the devices either breached inner or outer package trays or seal integrity was lost.
Nanosphere has recieved reports related to an unacceptable increase in initial no-call rate when performing the Verigene CYP2C19 Nucleic Acid Test (2C19), which has been confirmed through internal testing.
Zimmer is recalling sterile-packaged implants and instruments packaged in six different package configurations due to packaging design verification test failures. Specifically, multiple test samples from each of the six configurations failed simulated distribution and shipping testing when the devices either breached inner or outer package trays or seal integrity was lost.
A vendor changed the manufacturing process of a component used in the canister ring that may affect the performance of the ring. The deficit display may be higher than the actual deficit when the fluid collection canister is fully loaded.