Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 14801–14820 of 27,462 recalls
Recalled Item: DX-D 600 Product Usage: The DX-D 600 system is a Recalled by Agfa N.V. Due...
The Issue: A supplier for the Agfa system noted a potential for the steel support...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Olecranon Hook Plate Recalled by TriMed Inc. Due to The firm has...
The Issue: The firm has become aware that the angled-hole of certain semi-tubular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassHunter Quantitative Analysis Software Recalled by Agilent Technologies,...
The Issue: When utilizing specific software versions of an LC/MS device, and Batch at a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECOTHERM NEO Recalled by Tec Com Gmbh Due to The action is being initiated...
The Issue: The action is being initiated due to potential installation of faulty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portable Suction Pump Recalled by Ohio Medical Corporation Due to The...
The Issue: The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P640 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVS Aria Cage Recalled by Stryker Spine Due to The anterior and posterior...
The Issue: The anterior and posterior markers on the cage were on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P655 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoFlex LAL Support Surface Recalled by Stryker Medical Division of Stryker...
The Issue: Certain 2860 IsoFlex LAL support surfaces were assembled with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...
The Issue: A deterioration of performance was identified with influenza type B Enzyme...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest...
The Issue: Vials of the autoHDL/LDL Calibrator were shipped without a vial label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 140¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu Aura40 Standard Recalled by Besmed Health Business Corporation Due to...
The Issue: Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 Recalled by...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...
The Issue: The positive control on some tests of the lots did not appropriately react...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 11 mm x 260 mm Recalled by Zimmer Biomet,...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...
The Issue: The positive control on some tests of the lots did not appropriately react...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 260 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.