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. 1,145 recalls have been distributed to Washington in the last 12 months.
Showing 7381–7400 of 29,208 recalls
Recalled Item: FoundationOne Liquid CDx (F1LCDx) Recalled by Foundation Medicine, Inc. Due...
The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx (F1CDx) Recalled by Foundation Medicine, Inc. Due to...
The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...
The Issue: There is a potential for separation at the male connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...
The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...
The Issue: The power backup battery, under certain conditions, may exhibit reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...
The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...
The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller CUSHING MICRO BIPOLAR FORCEPS 0.7MM TIP Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT Recalled...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller HARDY BAYONET BIPOLAR FORCEPS WITH STOP Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller JEWELERS BIPOLAR FORCEPS 0.4MM TIP Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller GERALD BAYONET IRRIGATING BIPOLAR FORCEPS 1.0MM TIP...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller" SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.