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 2380123820 of 51,768 recalls

DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Phenol 10% Injection Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Tri-Mix 50:30:1 Recalled by Anderson Compounding Pharmacy,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2019· Olympus Corporation of the Americas

Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...

The Issue: There is a potential for the single use suction valve to come apart and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Incorrect part description contained on an additional label placed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Dornier Medtech America, Inc.

Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...

The Issue: Pin hole package failures compromising sterility of product

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

Class II — Potential Health HazardOngoing
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Dairy & Corn Free Bread Mix 19oz Recalled by Wholesome...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Banana Bread Mix 14oz Recalled by Wholesome Treats, Inc....

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Classic Herb Bread Mix 19oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Yeast Free Bread Mix 18.1oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Black Bean Brownie Mix 14oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 31, 2019· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope Recalled by Verathon, Inc. Due to A...

The Issue: A typographical error in the Operations & Maintenance Manual incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2019· Integra Limited

Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...

The Issue: Stability did not meet acceptance criteria for visual appearance during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2019· Thoratec Corp.

Recalled Item: Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief Recalled by...

The Issue: Outflow Graft leaking at the pump connection during the implantation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2019· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to...

The Issue: Outflow Graft leaking at the pump connection during the implantation...

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

Class II — Potential Health HazardOngoing
DrugMarch 29, 2019· X-Gen Pharmaceuticals Inc.

Recalled Item: Clonidine HCL Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Labeling: Label Error on Declared Strength: Side carton panel incorrectly...

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

Class III — Low RiskOngoing
Refund