The firm was manufacturing acidified foods without a license.
All Recalls
95,102 total recalls in our database
Peppered & Smoked Steelhead, Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67332 9
Sockeye Suzys Fish
Product has the potential to be contaminated with Clostridium botulinum.
The firm was manufacturing acidified foods without a license.
Smoked Sturgeon, Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67262 9
Sockeye Suzys Fish
Product has the potential to be contaminated with Clostridium botulinum.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
Failed Impurities/Degradation Specifications: High out of specification test result for impurities during stability testing.
Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as Docusate Calcium 240mg.
Penicillin Cross Contamination: Potential for products to be cross-contaminated with penicillin.
HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 10 cap/blister, 100-count carton, Rx only, Packaged and Distributed by American Health Packaging Columbus, Ohio 43217, NDC 68084-0398-01
Amerisource Health Services
Presence of Particulate Matter
Large objects with fine resolution are potentially displayed cropped when imported into Adaptive Hybrid Surgery Analysis version 1.0.0
Batteries found unresponsive after storage, not recognized by main device, and are perpetually enabled.
PMMA is listed as a material on the label but the product does not contain PMMA.
This correction to the da Vinci Xi I&A User Manual communicates proper use of the da Vinci Xi 8 mm Endoscopes in combination with the da Vinci 8 mm and 12 mm cannulae, cannula reducers, and monopolar energy instruments. It informs customers of scenarios that may result in unintended patient harm due to capacitive coupling from monopolar energy sources.
Batteries found unresponsive after storage, not recognized by main device, and are perpetually enabled.
Product on the package label did not match what was inside the package. The label was for part number 00-2359-058-35 (Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58mm Length) lot number 62918019 while the product inside the package was part number 00-2359-014-24 (Zimmer Periarticular Locking Plate System 2.4mm Locking Screw 14mm Length) lot number 62896038.