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. 2,552 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,552 in last 12 months

Showing 1410114120 of 47,654 recalls

Medical DeviceOctober 22, 2021· Atrium Medical Corporation

Recalled Item: The Ocean Water Seal Chest Drain is a plastic Recalled by Atrium Medical...

The Issue: Inadequate/inappropriate Set-Up Instructions, which may result in delay in...

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

Class II — Potential Health HazardOngoing
FoodOctober 21, 2021· Onions 52

Recalled Item: 5# (LB) Ctn (box) Jumbo Red Onions Recalled by Onions 52 Due to Potential...

The Issue: Voluntary recall due to possible contamination with Salmonella Oranienburg...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2021· Onions 52

Recalled Item: 40# (LB) Ctn (box) Jumbo Yellow Onions Recalled by Onions 52 Due to...

The Issue: Voluntary recall due to possible contamination with Salmonella Oranienburg...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2021· Onions 52

Recalled Item: 12 count per 2 lb. mesh sacks with Recalled by Onions 52 Due to Potential...

The Issue: Voluntary recall due to possible contamination with Salmonella Oranienburg...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of Recalled...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of Recalled...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
DrugOctober 20, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Gatifloxacin Ophthalmic Solution Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Failed Stability Specifications: Out-of-specification results observed in a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen ceiling with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor with software VD12- angiography systems developed for Recalled...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane with software VD12-angiography systems developed for single...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor with software VD12-angiography systems developed for single...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing