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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,459 in last 12 months

Showing 2378123800 of 27,451 recalls

Medical DeviceMarch 18, 2014· Energizer Personal Care

Recalled Item: Playtex Nurser Deluxe Double Electric Breast Pump Recalled by Energizer...

The Issue: Some of the power adapters outer casings may become loose and separate,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· SCM True Air Technologies LLC

Recalled Item: MaXair True Low Air Loss Mattress Replacement System Recalled by SCM True...

The Issue: The firm is recalling the products due to lack of design controls, lack of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· SCM True Air Technologies LLC

Recalled Item: ECATS E 850 Bariatric Bed Recalled by SCM True Air Technologies LLC Due to...

The Issue: The firm is recalling the products due to lack of design controls, lack of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Arjo Hospital Equipment AB

Recalled Item: ArjoHuntleigh Contoura C1000 series beds are designed to accommodate...

The Issue: There is a low but existing entrapment risk for a patient being treated on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-70. Product Usage: intended...

The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Philips Medical Systems, Inc.

Recalled Item: Digital Diagnost Recalled by Philips Medical Systems, Inc. Due to The...

The Issue: The footboard of Patient support for stitching can be fixed in upper...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· 3M Company - Health Care Business

Recalled Item: 3M" Steri-Vac" Gas Sterilizer/Aerators Recalled by 3M Company - Health Care...

The Issue: Recently, 3M received a single report of a potential exposure to Ethylene...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-80. Product Usage: intended...

The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...

The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...

The Issue: The products are labeled as sterile but were not sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The products are labeled as sterile but were not sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm)...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing