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. 2,665 recalls have been distributed to Washington in the last 12 months.
Showing 22761–22780 of 51,768 recalls
Recalled Item: Versa - Kath Mini Kit Recalled by Epimed International, Inc. Due to Mislabeling
The Issue: Mislabeled - The product's labeling contains an incorrect size for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versa - Kath Mini Kit Recalled by Epimed International, Inc. Due to Mislabeling
The Issue: Mislabeled - The product's labeling contains an incorrect size for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by...
The Issue: The products' cut, coagulate, or blend function may not operate with the use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotemax (loteprednol etabonate ophthalmic gel 0.5%) Recalled by Bausch &...
The Issue: Failed Stability Specifications: Out of specification for viscosity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: da Vinci Surgical System Recalled by Intuitive Surgical, Inc. Due to One da...
The Issue: One da Vinci Xi Endoscope Controller in the field was improperly calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS...
The Issue: Potentially Biased Results using VITROS Chemistry Products GLU Slides
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: Battery short-run times and unanticipated stoppage may be due to user not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ocean Supreme and Yaquina Bay IQF shrimp meat Recalled by California...
The Issue: The product was recalled because there was a foreign object found inside...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EQUISTREAM¿ XK Long-Term Hemodialysis Catheter....
The Issue: Incorrect Peel-Apart Introducer Sheath in Kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM¿ XK Long-Term Hemodialysis Catheter....
The Issue: Incorrect Peel-Apart Introducer Sheath in Kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 Recalled by...
The Issue: Device vented gas below the stated pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.