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. 2,653 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,653 in last 12 months

Showing 2436124380 of 51,768 recalls

Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Sof-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Kwart Retro-Inject Ureteral Stent Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Wire Guide Recalled by Cook Inc. Due to The wire guide may be incorrectly...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Urethral Dilator Set Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Roadrunner Hydrophilic PC Wire Guide Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Bentson PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Angled Tip Ureteral Catheter Set Recalled by Cook Inc. Due to The wire guide...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Heavy Duty PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Malecot Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Pigtail Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Universa Soft Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Sof-Flex Multi-Lenqth Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Fixed Core Straight Safety Wire Guide Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Wilson-Cook Medical Inc.

Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...

The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 3, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to...

The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 3, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Vecuronium Bromide for Injection 10 mg* Recalled by Sun Pharmaceutical...

The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 2, 2019· Baxter Healthcare Corporation

Recalled Item: Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5%...

The Issue: Lack of Assurance of Sterility: Confirmed customer complaints for leaks on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: CGMP Deviations: Product complaints received indicating reconstituted...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials Recalled...

The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: CGMP Deviations: Product complaints received indicating reconstituted...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund