Product Recalls in District of Columbia

Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,610 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,610 in last 12 months

Showing 1038110400 of 27,451 recalls

Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x9" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 6"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS PST Meters- IVD (Patient Self-Testing) measures blood-clotting...

The Issue: Possible Misinterpretation of Displayed Measuring Units from INR to %Quick...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Prof (Professional) Meters- IVD professional healthcare...

The Issue: Possible Misinterpretation of Displayed Measuring Units from INR to %Quick...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 5"x15" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 3"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 4"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Beckman Coulter Inc.

Recalled Item: MicroScan Pos MIC Panel Type 34 - Product Usage: For Recalled by Beckman...

The Issue: Due to a customer report and internal investigation, it was confirmed that a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm x10mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Biomet, Inc.

Recalled Item: Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled...

The Issue: Incorrect bolt -tibial bolts in package instead of femoral bolts may delay...

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

Class II — Potential Health HazardOngoing