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 30481–30500 of 50,914 recalls
Recalled Item: SmartMonitor 2 PS/PSL Recalled by Circadiance LLC Due to Circadiance has...
The Issue: Circadiance has determined that it is possible for certain Smart Monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LapSac Introducer Set Recalled by Cook Inc. Due to COOK Medical is...
The Issue: COOK Medical is initiating a voluntary recall of multiple products because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Willscher Vas Skewers Recalled by Cook Inc. Due to COOK Medical is...
The Issue: COOK Medical is initiating a voluntary recall of multiple products because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Needle Recalled by Cook Inc. Due to COOK Medical is...
The Issue: COOK Medical is initiating a voluntary recall of multiple products because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine HCI Injection Recalled by PAR Sterile Products LLC Due to...
The Issue: Crystallization: due to the presence of white, crystalline particulates,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Frozen Wild Shrimp Burgers Recalled by Unisea Inc. Due to Shrimp Burgers are...
The Issue: Shrimp Burgers are recalled because the Ingredients statement declared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TI Transport Monitor/Module Battery Pack Product Usage: intended for...
The Issue: Mindray has received two reports from outside the United States that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM IM NAIL 14MMDX30CM LEFT Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FXII SC TUBE PLT 90DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z NAIL PF 14MM X 46CM UNIV Z NAIL GT Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II STD TUBE 130DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM IM NAIL 15MMDX30CM Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIBIAL I/M NAIL 15MMDX26CM Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 BROAD SCP PLT 26-H STER Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F IM NAIL 10MMDX48CM LG Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Recalled...
The Issue: Potential sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol Transdermal System) 0.1 mg per day Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for peel force from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acyclovir Tablets Recalled by Hetero USA Inc Due to Presence of Foreign...
The Issue: Presence of Foreign Substance: human hair melded into tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Organic Veda brand Ginger Powder Recalled by Lords Organics Llc Due to...
The Issue: Lord Organics is recalling ginger powder because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.