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. 2,840 recalls have been distributed to Washington in the last 12 months.
Showing 1261–1280 of 29,208 recalls
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System Bardex I.C. Complete Care Infection Control...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray Recalled by...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant...
The Issue: Measles IgM Test Kit lacks premarket approval or clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Pack Recalled by O&M HALYARD INC Due to Surgical drape packs may...
The Issue: Surgical drape packs may have open seals, which may compromise the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle 3 with TumorLOC Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: Due to software issue, Radiation Therapy Planning system may provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOPS Inserter Recalled by PREMIA SPINE LTD Due to Potential for missing pins...
The Issue: Potential for missing pins at tip of inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Processor Recalled by Pentax of America Inc Due to...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromophare Surgical Light System Recalled by Stryker Communications Due to...
The Issue: Surgical lights have stress lines forming on the powder coating, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosthesis Head B Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Inconsistent size terminology and color coding used on labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Trial Head Brown Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: Inconsistent size terminology and color coding used on labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Operating Tables Model Numbers: (1) 770001A0 Recalled by MAQUET GMBH...
The Issue: Under certain conditions, such as the simultaneous use of the operating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic...
The Issue: Specific lots of reprocessed electrophysiology catheters may contain small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Novum IQ Large Volume Pump Recalled by Baxter Healthcare Corporation...
The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mensio Workstation (Vascular Fenestrated) software Recalled by PIE Medical...
The Issue: When fenestrated analysis with clock measurements is started in diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum Duo Infusion System Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical identified two sequences of programming events and alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.