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. 2,685 recalls have been distributed to Oregon in the last 12 months.
Showing 281–300 of 50,914 recalls
Recalled Item: Medline Convenience Kits: 1) ROBOTIC GYN CDS-1 Recalled by Medline...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT Recalled by Medline...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) ADMIT KIT Recalled by Medline Industries, LP...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) PICC LINE TRAY Recalled by Medline Industries,...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Surgical Drapes: 1) SHEET Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS Recalled by...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) ARTHROSCOPY CDS Recalled by Medline Industries,...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use Sphincterotome V (Distal Wire guided) Model/Catalog...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX M150 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HerbsForever- Hingwastika Churna Recalled by Herbs Forever Due to Undeclared...
The Issue: Potential undeclared allergen ingredient (Wheat)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OXIRIS SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a potential...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HerbsForever- Gastro Care Recalled by Herbs Forever Due to Undeclared Allergen
The Issue: Potential undeclared allergen ingredient (Wheat)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PRIMSAFLEX M100 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.