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. 2,469 recalls have been distributed to Washington in the last 12 months.
Showing 44821–44840 of 51,768 recalls
Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239...
The Issue: GE Healthcare has recently become aware of potential safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10" Hemoglobin Testing System Recalled by Bio-Rad Laboratories, Inc. Due...
The Issue: On a rare occasion the D-10 software might generate an extra result by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to...
The Issue: Labeling discrepancy.The label states that the implantable port contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...
The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
The Issue: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475630 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm Recalled by...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475625 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet Recalled by...
The Issue: Hospira identified an incorrect lower lid (set component) had been supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿/Apollo" Knee: M/B PAT SZ0 NATURAL-KNEE M/B PAT SZ1...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II Posterior Stabilized (P.S.) Condylar Tibial Inserts: N-K II...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II - Unicompartmental Knee Prosthesis: CONG TIB INS SZ1/2...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Knee Tibial Baseplate/Knee Tibial Insert: CONG TIB INS SZ0/19MM...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ N-K II DOMED ALL-POLY PAT Recalled by Zimmer, Inc. Due to A...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOST Options" System (MOST) HINGED TIB INS SZ 1 16MM Recalled by Zimmer,...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ Congruent Tibial Insert with Screw: SF-CON TIB INS LT Recalled...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.