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. 2,844 recalls have been distributed to Washington in the last 12 months.
Showing 301–320 of 51,768 recalls
Recalled Item: PRISMAFLEX ST100 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXIRIS SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a potential...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX M150 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX ST150 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raz-AT (Attendant Tilt) Mobile Shower Commode Chair Recalled by Raz Design...
The Issue: Due to a modification by a vendor and may be reinstalled without properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer STERILE saline wound wash Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sterile Saline Wound Wash Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION Recalled by Medline...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n)...
The Issue: Potential risk of Quality Control failures and/or false resistant antibiotic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lanreotide Injection Recalled by Cipla USA, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. Recalled by AVID Medical,...
The Issue: Tyvek bag seal issue which may compromise sterility of the kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioGlo Fluorescein Sodium Ophthalmic Strips USP Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bio Glo Fluorescein Sodium Ophthalmic Strips USP Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.