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. 1,777 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,777 in last 12 months

Showing 4722147240 of 51,768 recalls

Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Surgeon Side Cart Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Dual Camera Controller Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Instrument Control Box Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597603110 Articular Surface AC ART SURF 34/STRIPED YEL 10 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597201131 Femur CR POR SURF HDN FEM CO-NID AML Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597204109 Articular Surface CR ART SURF 56/STRIPE GRN 9 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems)....

The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00598706201 Provisional CRA FEM PROV/CUT GDE SZ BML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597103110 Provisional CR ART SURF PROV 34/STR YEL 10 Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Medtronic is recalling...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90597004109 Articular Surface CR ART SURF AE56/STR GRN 09MM Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597102010 Provisional CR ART SURF PROV 12/PURPLE 10 Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597502010 Provisional AC ART SURF PROV 12/PUR 10 Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 10 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597602010 Articular Surface AC ART SURF 12/PUR 10 Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597001131 Femur CR PRC SURF HDN FEM CO-NID AML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597601201 Femur CRA PRECOAT FEM COMP SIZE B/L Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing