Product Recalls in Oregon
Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,544 recalls have been distributed to Oregon in the last 12 months.
Showing 17861–17880 of 28,488 recalls
Recalled Item: Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP PRIMARY STEM 8MM MINI Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM LT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length Recalled by Zimmer...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS CEMENTED IM STEM 12X150 Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Bullet Tip 2.4 Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP 12MM HUM FRAC STEM MACRO Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER OPTION TYPE 1 TPR SLEVE -6 Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM RT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHO POR FMRL NC 9X125 Recalled by Zimmer Biomet, Inc. Due to Possibility...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER BIOLOXD OPTION HD 32MM Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.