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. 1,649 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
1,649 in last 12 months

Showing 4320143220 of 47,654 recalls

DrugJune 21, 2013· Tween Brands Inc

Recalled Item: I love to shop Justice Recalled by Tween Brands Inc Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: Shine from within blueberry Anti bac Justice Recalled by Tween Brands Inc...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: FOLLOW YOUR DREAMS! Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: TODAY IS AWESOME! Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: I MUSTACHE YOU TO BE MY BFF Justice Recalled by Tween Brands Inc Due to...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: GIRLS ROCK Justice Recalled by Tween Brands Inc Due to Labeling: Label Error...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: Grapefruit anti bac Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: yum yum bubble gum Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: Believe in Yourself Strawberry Anti bac Justice Recalled by Tween Brands Inc...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: I LOVE BACON Justice Recalled by Tween Brands Inc Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 20, 2013· Haemonetics Corporation

Recalled Item: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose...

The Issue: Research Use Only (RUO) parameters were included in TEG 5000 User Manual.

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

Class II — Potential Health HazardOngoing
FoodJune 20, 2013· Beta Labs

Recalled Item: Oxyphen XR Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: RED VIPERS Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: PHEnFX (TM) Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: PHENTALENE (TM) Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 19, 2013· Astellas Pharma US Inc

Recalled Item: AmBisome (amphotericin B) liposome for injection Recalled by Astellas Pharma...

The Issue: Lack of Assurance of Sterility; Astellas Pharma US, Inc. is performing a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Suction Wand Recalled by Edwards Lifesciences, LLC Due...

The Issue: Edwards is recalling certain lots of Rigid Suction Wands because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Philips Healthcare Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Healthcare...

The Issue: The MRx may deliver a non-synchronized cardioversion shock resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The...

The Issue: GE Healthcare has recently become aware of a potential safety issue with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW Recalled by Zimmer,...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing