Product Recalls in Washington
Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,432 recalls have been distributed to Washington in the last 12 months.
Showing 51361–51380 of 51,768 recalls
Recalled Item: Sunny Boy Peanut Butter. Product is labeled in part: 6/5 Recalled by...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product is 1 oz Peanut Butter. 1 oz pouch labeled Recalled by Sunshine...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sunny Boy Low Sodium/ Low Salt Peanut Butter. Product is Recalled by...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product is 2 oz Peanut Butter. 2 oz pouch labeled Recalled by Sunshine...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sunny Boy NoSalt Peanut Butter. No label was provided by Recalled by...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product is 50 lb Bag Peanut Butter. Product Case is Recalled by Sunshine...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Carescape Patient Data Module with v2.0 software used Recalled...
The Issue: GE Healthcare became aware of two issues with the Patient Data Module using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle Recalled by...
The Issue: A Discrepancy was found on Hitachi AST (HA7 61) package insert. Limitations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Advansys Medial Lisfranc Plate (MLP) Recalled by Integra...
The Issue: Incorrect technique applied may cause potential rupture of the tibialis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The finger cots are made out of natural rubber. They Recalled by Afassco Inc...
The Issue: The firm is initiating a field correction because the product(s) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection Recalled by...
The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection Recalled by...
The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CaviCide Recalled by Metrex Research, LLC. Due to Metrex Research is...
The Issue: Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow P2Y12 Assay Recalled by Accumetrics Inc Due to The recall was...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow System Recalled by Accumetrics Inc Due to The recall was initiated...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.