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. 1,730 recalls have been distributed to Oregon in the last 12 months.
Showing 49521–49540 of 50,914 recalls
Recalled Item: AUTOMIX 3+3 Compounder System Recalled by Baxter Healthcare Corp. Due to...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX Plus High Speed Compounder System Recalled by Baxter Healthcare...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX 3+3 Compounder with Accusource Monitoring System Recalled by Baxter...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX High Speed Compounder System Recalled by Baxter Healthcare Corp. Due...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The NCB Polyaxial Locking Plate System NCB screws 26mm: 02.03155.026...
The Issue: Zimmer investigation following a complaint found one lot of NCB Polyaxial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Dynamics Version 9.5 Recalled by Siemens Medical Solutions, USA, Inc...
The Issue: If multiple uncompressed images/clips are sent to the syngo Dynamics server,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a number of potential issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD Recalled...
The Issue: The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage TOX Drug Screen 9 Panel Recalled by Alere San Diego, Inc. Due...
The Issue: Alere San Diego is recalling Alere Triage TOX Drug Screen because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Organic Mild Salsa Recalled by Pulmuone Wildwood Inc Due to The...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Organic Medium Salsa Recalled by Pulmuone Wildwood Inc Due to The...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Hot Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.