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. 1,737 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls

1,737 in last 12 months

All Food Drug Medical Device Consumer Product Vehicle

Showing 33201–33220 of 47,654 recalls

Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing

Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing

Medical DeviceMarch 7, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Estradiol II Elecsys and cobas e analyzers 190 Recalled by Roche Diagnostics...

The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...

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

Class II — Potential Health HazardOngoing

Medical DeviceMarch 7, 2016· MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK

Recalled Item: VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear...

The Issue: In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect...

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

Class II — Potential Health HazardOngoing

Medical DeviceMarch 7, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Estradiol III Recalled by Roche Diagnostics Operations, Inc. Due to Due to...

The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...

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

Class II — Potential Health HazardOngoing

Medical DeviceMarch 4, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: The Spectra-System Dental Implant 2008 system is comprised of dental...

The Issue: Implant Direct Sybron Manufacturing, LLC is recalling GoDirect Implants...

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

Class II — Potential Health HazardOngoing

Medical DeviceMarch 4, 2016· C.R. Bard, Inc.

Recalled Item: BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management...

The Issue: Complaints were received of restricted/inaccurate flow rate.

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

Class II — Potential Health HazardOngoing

Medical DeviceMarch 4, 2016· Vascular Solutions, Inc.

Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...

The Issue: Vascular Solutions became aware of a potential problem with the click...

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

Class I — Serious Health HazardOngoing

FoodMarch 4, 2016· Materne North America Corp

Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...