Ortho-Clinical Diagnostics VITROS 5600 Integrated System -Software V3.3.2 & below Product recall — FDA Z-1287-2019
Luminometer Malfunction May Cause Inability to Process MicroWell Assays on VITROS Systems
Complete FDA and NHTSA recall records dated in May 2019.
These records include useful source details for the selected month.
Luminometer Malfunction May Cause Inability to Process MicroWell Assays on VITROS Systems
Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
Luminometer Malfunction May Cause Inability to Process MicroWell Assays on VITROS Systems
Luminometer Malfunction May Cause Inability to Process MicroWell Assays on VITROS Systems
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary recall of El Guapo Chile Habanero and Chili Pasilla-Ancho pouches due to unlabeled peanut allergen.
Product is being recalled due to the presence of foreign material (hard plastic).
Undeclared sulfites.
Dried whole Elderberries are recalled due to glass fragments contamination.
Imported Frozen Poppy Seed bread contains elevated levels of Morphine and Codeine.
Product is being recalled due to the presence of foreign material (hard plastic).
Product is recalled due to glass fragment contamination
Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary recall of El Guapo Chile Habanero and Chile Pasilla-Ancho pouches due to unlabeled peanut allergen.
Product may contain foreign material
Product may be contaminated with Salmonella.
Elite Spice, Inc. has initiated a recall of Basil Olive Oil Flavored Tortilla Seasoning, Lot Number:1-310242, Units Per Case: 1, Weight Per Package: 50 pounds because Elite Spice produced a…
Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg
Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg
Product Mix-Up: Customer complaint that their carton labeled as Fentanyl Transdermal Systems, 12 mcg/h contained five patches labeled and containing 50 mcg/h.
Lack of Sterility Assurance: Microbial growth detected during a routine simulation of the manufacturing process, which represents the potential introduction of microorganisms into the…
Mazda North American Operations (Mazda) is recalling certain 2019 Mazda3 vehicles. Due to incorrect programing, the passenger air bag deactivation indicator light may erroneously turn off…
BMW of North America, LLC (BMW) is recalling certain 2016-2019 X1 sDrive28i and X1 xDrive28i vehicles. In the event of a crash where the occupants head contacts the B-pillar, the pillar may…
Potential risk of scans being aborted when using the optional Dual Spiral Dual Engery mode due to a software issue found in syngo CT VB10A for the Siemens Healthineers CT scanners with a…
Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in 316 and lower and Atellica IM aTG kit lots ending in 317 and lower when compared to the standardization to World…
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.