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. 2,698 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,698 in last 12 months

Showing 2160121620 of 51,768 recalls

Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For Recalled...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1500-04-S. For...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1300-04-S. For...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a / 980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Exactech, Inc.

Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...

The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2019· West-Ward Columbus Inc

Recalled Item: Oxcarbazepine Oral Suspension Recalled by West-Ward Columbus Inc Due to...

The Issue: Failed Impurities/Degradation Specificattion

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Darmerica, LLC

Recalled Item: Quinacrine Dihydrochloride (98.25%) Recalled by Darmerica, LLC Due to Label...

The Issue: Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 6, 2019· Cardinal Health dba Specialty Pharmaceutical Services

Recalled Item: Nucala (mepolizumab) Injection Recalled by Cardinal Health dba Specialty...

The Issue: Temperature Abuse; Product stored and shipped outside of labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Torrent Pharma Inc.

Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High Out Of Specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Mylan Pharmaceuticals Inc....

The Issue: Failed Impurities/Degradation Specifications:OOS for unknown impurity.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 6, 2019· Pfizer Inc.

Recalled Item: Bacteriostatic Water for Injection Recalled by Pfizer Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 6, 2019· Medline Industries Inc

Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...

The Issue: The recall is being conducted due to a potential defective component on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2019· CooperSurgical, Inc.

Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...

The Issue: The touchpad may not work properly after cleaning.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing