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. 2,765 recalls have been distributed to Washington in the last 12 months.
Showing 15121–15140 of 51,768 recalls
Recalled Item: Artesunate for Injection Recalled by AMIVAS (US), LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Air filter failed post integrity test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES Recalled by O&M...
The Issue: All lots of the glove may discolor and lose elasticity upon aging, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Glucagon Emergency Kit for Low Blood Sugar Recalled by Eli Lilly & Company...
The Issue: SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FAIRLIFE MILK 8OZ / 6PK CHOCOLATE (multi-pack format of small Recalled by...
The Issue: Product has potential for spoilage and lack of commercial sterility.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) Recalled...
The Issue: 3D-RA is a reconstruction software product that can be used with the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Permobil TiLite Recalled by TiSport, Llc Due to Some affected wheelchairs,...
The Issue: Some affected wheelchairs, with transit tie downs, that are used as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-Ray System Recalled by Philips...
The Issue: When the user presses or releases both the APC (accept) button and the Float...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error, the software can produce an incorrect interpretation of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinician Programmer Application (CPA) model A610 Clinician Software...
The Issue: A software anomaly may occur with the clinician programmer application.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIMPLEXA COVID-19 Positive Control Pack Recalled by DiaSorin Molecular LLC...
The Issue: Due to unapproved raw materials used in the manufacturing of Covid-19...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.