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. 2,766 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,766 in last 12 months

Showing 1384113860 of 51,768 recalls

Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· Canon Medical System, USA, INC.

Recalled Item: INFX-8000V. For radiographic and fluoroscopic studies and intervention....

The Issue: The fluoroscopic dose rate might exceed the conforming value during biplane...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Ysiosystem with VC10 software version Recalled by Siemens Medical Solutions...

The Issue: Siemens Healthineers has identified a software error in previous software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· SD Biosensor, Inc.

Recalled Item: STANDARD Q COVID-19 Ag Home Test STANDARD Q COVID-19 Ag Recalled by SD...

The Issue: Illegal importation of COVID-19 AG Test kits into the U.S. The COVID-19 Ag...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 31, 2022· B. Braun Medical, Inc.

Recalled Item: Dispensing Pins for Air Inlet Filter Recalled by B. Braun Medical, Inc. Due...

The Issue: This lot may have an elevated risk of leakage from the Air-Inlet Filter of...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2022· AMS Packaging Inc

Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...

The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 28, 2022· AMS Packaging Inc

Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...

The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 28, 2022· Esupplementsales, LLC

Recalled Item: HARD DAWN Recalled by Esupplementsales, LLC Due to Marketed Without an...

The Issue: Marketed Without an Approved NDA/ANDA: Firm was informed by Amazon that...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 28, 2022· CONAGRA BRANDS

Recalled Item: Wishbone Chunky Blue Cheese Dressing 24oz. bottle Recalled by CONAGRA BRANDS...

The Issue: Undeclared eggs

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 28, 2022· CONAGRA BRANDS

Recalled Item: Wishbone Thousand Island Dressing 15oz. bottle and 24 Recalled by CONAGRA...

The Issue: Undeclared eggs

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 28, 2022· B Braun Medical Inc

Recalled Item: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems....

The Issue: Firm learned of the potential for cracks to form in the conductivity sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2022· B Braun Medical Inc

Recalled Item: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems....

The Issue: Firm learned of the potential for cracks to form in the conductivity sensors...

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

Class II — Potential Health HazardOngoing