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. 2,629 recalls have been distributed to Washington in the last 12 months.
Showing 27261–27280 of 51,768 recalls
Recalled Item: Acadica Kratom: Red Suma 250g bags Recalled by Badger Botanicals LLC Due to...
The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acadica Kratom: Green Hulu 2 Kratom Recalled by Badger Botanicals LLC Due to...
The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acadica Kratom: Red Hulu 2 Recalled by Badger Botanicals LLC Due to...
The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1) Drainer Centesis Catheter Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centeze Centesis Catheter Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducers Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elite HV Introducer Recalled by Galt Medical Corporation Due to The products...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) TVS LPA Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ELITE HV Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TVS LPA Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Vascular Dilator Recalled by Galt Medical Corporation Due to The products...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N...
The Issue: The diameter of the drill sleeve guide raw material was found to be under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-M Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-C Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-C Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...
The Issue: The bottles are mislabeled with an incorrect part number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: Cross-contamination of samples has been reported when running the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...
The Issue: Possible transient electrical connection interruption between an HVAD System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...
The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.