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. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 28221–28240 of 50,914 recalls
Recalled Item: rHead Recon Stem Implant non-coated Recalled by Howmedica Osteonics Corp....
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radio Capitellum Small Recalled by Howmedica Osteonics Corp. Due to Revision...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: radial stem implant #3 (Sterile packed). Orthopedic implant for replacement...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer with FLEXQ module. Device intended for in vitro Recalled by...
The Issue: Due to misinterpretation of the barcode by the scanner, when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GMK knee system: designed for cemented use in total Recalled by Medacta...
The Issue: Medacta has observed a worldwide occurrence rate of post-operative insert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee Spacer Blocks To assist in partial knee Recalled by...
The Issue: Zimmer Biomet is conducting a medical device recall for the Persona Partial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensicare Green Surgical Glove Recalled by Medline Industries Inc Due to...
The Issue: Possible open seal on top portion of the package. Could cause breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tres Latin Foods Pupusas Recalled by Tres Latin Foods Due to Undeclared Milk
The Issue: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tres Latin Foods Kale & Pinto Bean pupusas Stuffed Corn Tortillas Recalled...
The Issue: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: diphenoxylate hydrochloride and atropine sulfate tablets Recalled by Pfizer...
The Issue: SUPERPOTENT: Weight variations resulting in tablets that are sub and super...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zoloft (sertraline HCl) tablets 25 mg* 30-count bottle Recalled by Pfizer...
The Issue: SUPERPOTENT: Weight variations resulting in tablets that are sub and super...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultrasound Transducer Recalled by Hitachi Medical Systems America Inc Due to...
The Issue: The ultrasound probe may not have adequate protection against electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST TERUMOBCT Recalled by Terumo BCT, Inc. Due to Certain lots of the...
The Issue: Certain lots of the Harvest Graft Delivery System GDP-10 Procedure Packs may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Gastrojejunostomy Set Product Usage: Intended for the...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bliss anti-stress formula Dietary Supplement Recalled by Market America Inc...
The Issue: Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset...
Recommended Action: Do not consume. Return to store for a refund or discard.