95,025 total recalls in our database
Teva Pharmaceuticals USA
Labeling: Incorrect or Missing Lot and/or Exp date on the individual transdermal pouches but not in the carton.
SCA Pharmaceuticals
Subpotent Drug: Out-of-Specification potency results at the 30-day stability timepoint.
cGMP Deviations.
West-Ward Columbus
Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code.
Failed Impurities/Degradation Specifications: Out of specification result observed in related substance test.
Failed Content Uniformity: bulk lot used to make these two lots was found to have failed content uniformity.
cGMP Deviations.
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.
An instrument failure mode that may result in a Blood Culture Gram Positive (BC-GP) or Gram Negative (BC-GN) false negative call.
The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
High rate of galling of one threaded component.
Incorrect manufacturer calibration
HF Acquisition Co.
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
HF Acquisition Co.
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.
Incorrect manufacturer calibration
Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.
HF Acquisition Co.
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
An instrument failure mode that may result in a Blood Culture Gram Positive (BC-GP) or Gram Negative (BC-GN) false negative call.