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. 2,624 recalls have been distributed to Washington in the last 12 months.
Showing 27921–27940 of 51,768 recalls
Recalled Item: CATHETER REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to There is...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12F MODIFIED Tesio CATHETER SET Recalled by Medical Components, Inc dba...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO lnfiniti Needle Guide Bracket. used for performing needle-guided (or...
The Issue: A cover failed leak testing during validation testing of new needle guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterzone 180 count bottle packaged in an amber plastic bottle Recalled...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Variety Pack Recalled by Pinks Bakery Seattle, Inc. Due to Coconut is listed...
The Issue: Coconut is listed in the ingredient statement but is not declared in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hippie Cookie Recalled by Pinks Bakery Seattle, Inc. Due to Coconut is...
The Issue: Coconut is listed in the ingredient statement but is not declared in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Life Change Fat Burner Recalled by Get The Tea Due to Get The Tea is...
The Issue: Get The Tea is notifying customers that Life Change Fat Burners contain soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thyroid Resilience 120 count bottle packaged in an amber plastic Recalled by...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pink flexible Recalled by Ikea North America Srvcs Inc Due to Possible Pest...
The Issue: Possible Pest Contamination at production facility.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: cobas b 221 AutoQC Module Complete Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 221<4>Roche OMNI S4 system Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221<6>Roche OMNI S6 system Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and Recalled...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 8FR 50cc Product Usage: The intra-aortic...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 30cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: F-T3SYSTEM Recalled by Allen Medical Systems Due to The recalling firm has...
The Issue: The recalling firm has become aware that the rail section clamps used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 56% 1 Day Silicone Hydrogel (-2.50) Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.