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. 2,624 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,624 in last 12 months

Showing 2848128500 of 51,768 recalls

FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED FISH CHUNKY WHITEFISH SPREAD 8 oz. Recalled by Rachael's...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Boston Salads Veggie Cream Cheese Spread Recalled by Rachael's Food...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Rachael's SPRINGFIELD SMOKED FISH STRAWBERRY CREAM CHEESE SPREAD Recalled by...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED FISH Smoked Chubs Recalled by Rachael's Food Corporation...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 11, 2017· Medical Action Industries Inc

Recalled Item: Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable Recalled...

The Issue: Product sterility potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Boston Scientific Corporation

Recalled Item: Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is Recalled...

The Issue: Potential polymer material degradation.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Philips Electronics North America Corporation

Recalled Item: digital x-ray detector ProGrade R1 - solid state X ray Recalled by Philips...

The Issue: It the WiFi connection between the SkyPlate detector and HP transfer point...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Sanofi Genzyme

Recalled Item: Synvisc-One ¿ (hylan G-F 20) Recalled by Sanofi Genzyme Due to Contamination...

The Issue: Contamination with Methylbacterium thiocyanatum

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Remel Inc

Recalled Item: Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum Recalled by Remel Inc...

The Issue: The serum may fail to agglutinate within the specified minimum reaction time.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c16000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c8000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and Recalled...

The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and Recalled...

The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Datex-Ohmeda, Inc.

Recalled Item: CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The...

The Issue: Potential for the display processor to experience an unexpected failure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ALTRUA 2 SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing