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. 2,584 recalls have been distributed to Washington in the last 12 months.
Showing 39141–39160 of 51,768 recalls
Recalled Item: Akttive High Performance Fat Burner Gold dietary supplement capsules...
The Issue: Marketed Without An Approved NDA/ANDA: Dietary supplements contains...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mometasone Furoate Ointment USP Recalled by Perrigo Israel Pharmaceuticals...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Intermezzo (zolpidem tartrate) Recalled by Purdue Pharma L.P. Due to Failed...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....
The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....
The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray....
The Issue: Electrostatic energy may be stored in Systems that can cause a short-cicuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS500 of an IACS Workstation Critical Care (Evita Infinity V500) Recalled by...
The Issue: The battery capacity of the optional PS500 of an IACS Workstation Critical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etac Relax wall mounted shower seat The Etac Relax is Recalled by Etac...
The Issue: The recalling firm has received reports of a malfunction of the Relax wall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery Recalled by...
The Issue: Stryker Sustainability Solutions has received reports indicating that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A gradient cable in the ACGD...
The Issue: A gradient cable in the ACGD cabinet may be missing a spacer that prevents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro-Mate Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfectum Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Electrical Clipper with Charging base The Electrical Surgical...
The Issue: Charging base of surgical clippers overheats and smokes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitroglycerin Transdermal System 0.2 mg/hr (10 cm2) Recalled by Kremers...
The Issue: Failed Impurities/Degradation Specifications: failed specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitroglycerin Transdermal System 0.4 mg/hr (18 cm2) Recalled by Kremers...
The Issue: Failed Impurities/Degradation Specifications: Two lots failed specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.