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. 2,040 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,040 in last 12 months

Showing 99619980 of 29,208 recalls

Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: HIGH PRESSURE TUBING Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: ELI 280 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD Recalled by Smiths Medical ASD Inc....

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: ELI 380 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Mark 910 LogiCal Recalled by Smiths Medical ASD Inc. Due to Specific lots of...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: ACE MDI Spacer with Small Mask - Product Usage: designed Recalled by Smiths...

The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Palm Cups - Product Usage: intended to be used to Recalled by Smiths Medical...

The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Gang Cath Lab Set Recalled by Smiths Medical ASD Inc. Due to Specific lots...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Soft Computer Consultants, Inc.

Recalled Item: SoftCytogenetics Recalled by Soft Computer Consultants, Inc. Due to Software...

The Issue: Software is given wrong results going out to HIS on test that had reruns.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: LogiCal Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific lots of...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Tubing with male luer lock adapter (Component) a. 76 cm Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...

The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Recalled by Nobel Biocare...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75...

The Issue: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show...

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

Class II — Potential Health HazardOngoing