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. 2,665 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,665 in last 12 months

Showing 2298123000 of 51,768 recalls

Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229001A Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811961 Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229002A Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811901 Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811910...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229034A Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811911 Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229035A...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
FoodMay 24, 2019· LAIRD SUPERFOOD INC

Recalled Item: Performance Mushrooms product is dried mushroom blend of 4 different...

The Issue: The product is incorrectly labeled with 14 mg of Iron and 78% DV when the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 24, 2019· Abbott Laboratories

Recalled Item: ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are...

The Issue: Presence of a time dependent, stability drift in patient and control results...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2019· Abbott Laboratories

Recalled Item: ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are...

The Issue: Presence of a time dependent, stability drift in patient and control results...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) CF 6.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) HVT 6.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan LTS Recalled by Teleflex Medical Due to This voluntary...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/HVT: 1) Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) Preformed 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing