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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,485 in last 12 months

Showing 1922119240 of 27,451 recalls

Medical DeviceJune 2, 2016· Arrow International Inc

Recalled Item: ARROW Recalled by Arrow International Inc Due to Arrow is recalling these...

The Issue: Arrow is recalling these products due to the possibility that although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2016· Parker Medical

Recalled Item: Parker Trach-Vac Endotracheal Tubes. Tyvek pouches Recalled by Parker...

The Issue: Parker Medical announces a voluntary field action for the Parker Trach-Vac...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Total T4 Reagent Pack Recalled by...

The Issue: Ortho-Clinical Diagnostics confirmed that sample results generated from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.221 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Screwdriver Blade Recalled by Synthes (USA) Products LLC Due to DePuy...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Hologic, Inc

Recalled Item: ATEC CANISTER. Suction Canister with Lid 490 cc. Recalled by Hologic, Inc...

The Issue: Cracks ATEC Canister Lids.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #311.039 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.212 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # SD313.011 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.232 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.231 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.250 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.946 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Ultrasound Video Bronchoscope The EB-1970UK Recalled by Pentax of America...

The Issue: The EB-1970UK Ultrasound Video Bronchoscope shipped between the clearance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # SD313.012 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Ti Button Plate 7 Holes Recalled by Synthes (USA) Products LLC Due...

The Issue: DePuy Synthes is voluntarily initiating a recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Draeger Medical, Inc.

Recalled Item: Oxylog 3000 Recalled by Draeger Medical, Inc. Due to Isolated episodes of...

The Issue: Isolated episodes of leakage at the check valve were found

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.211 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Pentax Video Bronchoscope Designed to be used with a Pentax Recalled by...

The Issue: Pentax America Inc. is recalling various bronchoscopes which contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color C2 60ml art. no. 681060. Product Usage: Recalled by...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing