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 2610126120 of 47,654 recalls

Medical DeviceJanuary 25, 2018· GE Healthcare

Recalled Item: Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with...

The Issue: Potential that one or more image series may be missing from an exam without...

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

Class II — Potential Health HazardOngoing
DrugJanuary 25, 2018· PD-Rx Pharmaceuticals, Inc.

Recalled Item: PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets...

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 25, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 mobile image-intensified fluoroscopic x-ray system Recalled by...

The Issue: Software update ("SW Update 3.2.1") is being implemented to address the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Liberty Select Cycler (SW v.2.8.7) Recalled by Fresenius Medical Care Renal...

The Issue: The recalling firm identified a software issue related to the Patient Line...

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

Class II — Potential Health HazardOngoing
DrugJanuary 24, 2018· JCB Laboratories LLC

Recalled Item: Cefuroxime Recalled by JCB Laboratories LLC Due to Subpotent Drug: The...

The Issue: Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.

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

Class III — Low RiskOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Panera Reduced-Fat Plain Cream Cheese Recalled by Panera, LLC Due to...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Panera Chive&Onion Reduced Fat Cream Cheese Spread Recalled by Panera, LLC...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Reduced-Fat Wild Blueberry Cream Cheese Recalled by Panera, LLC Due to...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Panera Reduced-Fat Honey Walnut Cream Cheese Recalled by Panera, LLC Due to...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 24, 2018· Bell Plantation Inc.

Recalled Item: Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic jars Recalled...

The Issue: Analytical results for generic non-pathogenic E. coli surpassed firm's...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Panera Plain Cream Cheese Recalled by Panera, LLC Due to Potential Listeria...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 23, 2018· 3M Company - Health Care Business

Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...

The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2018· 3M Company - Health Care Business

Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...

The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2018· Biomerieux Inc

Recalled Item: bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is Recalled by Biomerieux...

The Issue: Missing desiccant.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2018· Valeris Medical, LLC

Recalled Item: Apollo XT Suture Anchor Recalled by Valeris Medical, LLC Due to The label on...

The Issue: The label on Apollo XT 5.5mm Suture Anchor (part # XTS-5515; lots 2358,...

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

Class II — Potential Health HazardOngoing
DrugJanuary 22, 2018· Ascent Pharmaceuticals, Inc.

Recalled Item: Oxycodone Hydrochloride Tablets Recalled by Ascent Pharmaceuticals, Inc. Due...

The Issue: Labeling; Label Error Not Elsewhere Classified; label missing controlled...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 22, 2018· Astellas Pharma US Inc

Recalled Item: Mycamine (micafungin) for Injection 100 mg/vial Single-Dose Vial Rx only...

The Issue: Labeling: Label Error on Declared Strength

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2018· SIE AG, Surgical Instrument Engineering

Recalled Item: The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8...

The Issue: This Correction is being initiated based on a customer complaint received on...

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

Class II — Potential Health HazardOngoing
DrugJanuary 19, 2018· Flawless Beauty LLC

Recalled Item: Reiki Glutathione Whitening kits Recalled by Flawless Beauty LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2018· Flawless Beauty LLC

Recalled Item: Sterilized water for injections BP Recalled by Flawless Beauty LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily...

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

Class II — Potential Health HazardOngoing
Refund