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. 2,711 recalls have been distributed to Washington in the last 12 months.
Showing 20761–20780 of 51,768 recalls
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...
The Issue: Labeling mix-up - Indications on product label are incorrect.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...
The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breakstones 4% Milkfat Small Curd Cottage Cheese Recalled by THE KRAFT HEINZ...
The Issue: Potential presence of pieces of red plastic and metal that may have been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breakstones 4% Milkfat Large Curd Cottage Cheese Recalled by THE KRAFT HEINZ...
The Issue: Potential presence of pieces of red plastic and metal that may have been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breakstones 2% Milkfat Lowfat Large Curd Cottage Cheese Recalled by THE...
The Issue: Potential presence of pieces of red plastic and metal that may have been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Revaclear Capillary Dialyzer 300 Recalled by Baxter Healthcare Corporation...
The Issue: There is the potential presence of particular matter in the header caps of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PneumoDart Recalled by Tytek Medical Inc Due to A defect involving an...
The Issue: A defect involving an occluded needle was discovered during a training exercise.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm" O2 Imaging System Recalled by Medtronic Navigation, Inc.-Littleton...
The Issue: Due to a manufacturing issue affecting particular O-arm" O2 Imaging Systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment...
The Issue: The AIA-2000 bar code scanners depend on the quiet zone to help identify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130 Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HardyCHROM MRSA Recalled by Hardy Diagnostics Due to False Positive results...
The Issue: False Positive results due to the MSSA (methicillin-susceptible) strain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.