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. 2,470 recalls have been distributed to Oregon in the last 12 months.
Showing 26601–26620 of 50,914 recalls
Recalled Item: Acadica Kratom: Red Hulu 2 Recalled by Badger Botanicals LLC Due to...
The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N...
The Issue: The diameter of the drill sleeve guide raw material was found to be under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-M Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-C Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-C Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...
The Issue: The bottles are mislabeled with an incorrect part number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: Cross-contamination of samples has been reported when running the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...
The Issue: Possible transient electrical connection interruption between an HVAD System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...
The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by AuroMedics Pharma LLC...
The Issue: Presence of Particulate Matter: confirmed customer report for presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ampicillin and Sulbactam for Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Presence of Particulate Matter: confirmed customer report of the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bob's Red Mill 100% Whole Wheat Bread Mix Recalled by Bob's Red Mill Natural...
The Issue: 100% Whole Wheat Bread Mix is recalled due to undeclared wheat in the label...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zeego Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q ceiling Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to After the...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.