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. 2,472 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,472 in last 12 months

Showing 2354123560 of 47,654 recalls

Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MC Recalled by GE Healthcare, LLC Due to A detector...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Luminex Corporation

Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...

The Issue: Potential to lead to a false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled by...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
FoodSeptember 13, 2018· Swanson Health Products, Inc

Recalled Item: Swanson Ultra Recalled by Swanson Health Products, Inc Due to Himalayan...

The Issue: Himalayan Crystal Salt may contain metal wire pieces.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 13, 2018· Roche Diagnostics Corporation

Recalled Item: CoaguChek¿ XS System Prothrombin time test: CoaguChek XS PT Test 2X24 Strips...

The Issue: Abnormally high INR test results with the affected CoaguChek test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 13, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System Recalled...

The Issue: The service manual was not updated at the time of the release of software...

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

Class II — Potential Health HazardOngoing
FoodSeptember 12, 2018· Swire Coca Cola USA

Recalled Item: Caffeine-Free Barq s Root Beer 12 Pack Recalled by Swire Coca Cola USA Due...

The Issue: Recalling Caffeine-Free Barq s Root Beer 12 Pack due to mislabeling.

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 12, 2018· CMP Industries, Llc

Recalled Item: IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1 Recalled by CMP...

The Issue: Foreign material in product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 3000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 1000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 2000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· CMP Industries, Llc

Recalled Item: Technoflux IMPAK Resina lfquida acrilica elastic Curado-Calor Tipo 1...

The Issue: Foreign material in product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 500 mL - Product Usage: Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Howmedica Osteonics Corp.

Recalled Item: Tritanium TL Steerable Inserter Recalled by Howmedica Osteonics Corp. Due to...

The Issue: The firm received complaints related to the locking mechanism on the...

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

Class II — Potential Health HazardOngoing