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. 2,469 recalls have been distributed to Washington in the last 12 months.
Showing 44221–44240 of 51,768 recalls
Recalled Item: Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Recalled...
The Issue: There is a potential fire hazard of certain Lithium-Ion batteries in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Ventilator Flexport Interface Recalled by Spacelabs...
The Issue: Spacelabs Healthcare is voluntarily recalling the Hamilton Galileo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems...
The Issue: Excessive usage of cleaning liquid on Siemens Ysio Systems may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000...
The Issue: Physio-Control has become aware of incidents where customers have attempted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROMETHAZINE HYDROCHLORIDE Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Presence of Foreign Tablets: Presence of atenolol 25 mg tablet mixed into...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Devon Supine Recalled by Covidien LLC Due to Straps may separate from the...
The Issue: Straps may separate from the foam pad.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Pneumatic and Electric Motor Systems. Intended for cutting and...
The Issue: Several attachments and handpieces failed to meet the expected sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACROLYTE Premie Dispersive Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed Corporation has received complaints regarding sparking, no output and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Post Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Rod Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS System Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a potential risk when using LANTIS OIS System client software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visitec Anterior Chamber Cannula Recalled by Beaver-Visitec International...
The Issue: Contains a sharp tip needle when the product should contain a blunt tip cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFRICAN BLACK ANT Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MOJO RISEN Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Black Ant Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemo-Stat Solution Recalled by Axcentria Pharmaceuticals, LLC Due to...
The Issue: Marketed without an Approved NDA/ANDA; product is being manufactured and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Velvet cake Recalled by Asian Bakery Due to Undeclared Wheat
The Issue: Cakes are being recalled due to undeclared wheat and soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bells cake Recalled by Asian Bakery Due to Undeclared Wheat
The Issue: Cakes are being recalled due to undeclared wheat and soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Marquiz cake Recalled by Asian Bakery Due to Undeclared Milk
The Issue: Cakes are being recalled due to undeclared milk, wheat and soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chernosliv cake Recalled by Asian Bakery Due to Undeclared Milk
The Issue: Cakes are being recalled due to undeclared milk, wheat and soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.