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. 1,904 recalls have been distributed to Washington in the last 12 months.
Showing 27921–27940 of 51,768 recalls
Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...
The Issue: Wire sets of certain devices were assembled with adhesive on the contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12F Tesio CATHETER SET (CUFF 32CM FROM TIP) Recalled by Medical Components,...
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 X 40CM TESIO CATHETER SET WITH "Y" ADAPTOR Recalled by Medical...
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 X 60CM TESIO CATHETER SET WITH "Y" ADAPTOR Recalled by Medical...
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 Tesio CATHETER SET (CUFF 22CM FROM TIP) Recalled by Medical Components,...
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: 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: TWO PART ADAPTER 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: 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: 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<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: 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<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: Atropine Sulfate Ophthalmic 1% Solution Recalled by Akorn, Inc. Due to...
The Issue: Failed Stability Specification: OOS low viscosity results discovered during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT 2.96oz (84g)...
The Issue: Mold growth on product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g) Recalled...
The Issue: Mold growth on product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Emerald brand Glazed Walnuts Recalled by Snyder's-Lance Inc. Due to...
The Issue: Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to...
Recommended Action: Do not consume. Return to store for a refund or discard.