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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,360 in last 12 months

Showing 4604146060 of 47,654 recalls

Medical DeviceAugust 28, 2012· Sekisui Diagnostics Llc

Recalled Item: Sekisui Spectrolyse PAI-1 Recalled by Sekisui Diagnostics Llc Due to...

The Issue: SPECTROLYSE PAI-1 activity assay producing lower than expected absorbance...

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

Class II — Potential Health HazardOngoing
DrugAugust 27, 2012· Samantha Lynn, Inc

Recalled Item: Reumofan Plus Tablets Recalled by Samantha Lynn, Inc Due to Undeclared Drug

The Issue: Marketed without an approved NDA/ANDA: Samantha Lynn Inc. is recalling...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 27, 2012· Zimmer, Inc.

Recalled Item: Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves...

The Issue: Trilogy Longevity Constrained Liner devices were packaged in incorrect...

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

Class II — Potential Health HazardOngoing
FoodAugust 25, 2012· Splendid Products

Recalled Item: Daniella Mangoes May be identified by Daniella sticker with a Recalled by...

The Issue: Firm is recalling certain lots of Daniella brand mangoes because they may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 25, 2012· Cinnabar Specialty Foods Inc

Recalled Item: Neera's Tikka Curry Rich and Creamy All Natural Simmering Sauce Recalled by...

The Issue: The product was recalled due to undeclared sub-ingredients of milk and soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Whey Protein Isolate Cross-Flow Microfiltration Recalled by MyoSci...

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Whey Protein Concentrate Recalled by MyoSci Technologies Inc. Due to...

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Whey Protein Isolate Cold-Filtration Recalled by MyoSci Technologies Inc....

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Hydrolyzed Whey Protein High Grade Recalled by MyoSci Technologies Inc. Due...

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Whey Protein Isolate MicroFiltration Recalled by MyoSci Technologies Inc....

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 24, 2012· Iradimed Corporation

Recalled Item: The brand name is MRidium Series 1000 MR Infusion Sets Recalled by Iradimed...

The Issue: Iradimed Corporation is recalling MRidium Series 1000 MR Infusion Sets, Type...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: MX 16-slice CT Scanner System Recalled by Philips Medical Systems...

The Issue: On August 24, 2012 the firm recalled the MX 16-slice after discovering that...

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

Class II — Potential Health HazardOngoing
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights Recalled by Evol Nutrition Due to Marketed Without an Approved...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights for Her Recalled by Evol Nutrition Due to Marketed Without an...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Ferring Pharmaceuticals Inc

Recalled Item: Novarel¿ (Chorionic Gonadotropin for injection Recalled by Ferring...

The Issue: Labeling; incorrect or missing insert; Warnings portion of the Package...

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

Class III — Low RiskOngoing
Refund
FoodAugust 23, 2012· Safeway Inc

Recalled Item: "SAFEWAY farms White Sliced Mushrooms***DISTRIBUTED BY SAFEWAY...

The Issue: Champs 8 oz Sliced White Mushrooms are recalled due to potential...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 23, 2012· King Systems Corp.

Recalled Item: Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia...

The Issue: King Systems received a customer complaint indicating that the customer had...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 23, 2012· Biomet, Inc.

Recalled Item: Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Recalled by...

The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2012· Biomet, Inc.

Recalled Item: Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Recalled by...

The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2012· Viscot Medical LLC

Recalled Item: Dual Tip Marker Recalled by Viscot Medical LLC Due to Dual Tip Marker has...

The Issue: Dual Tip Marker has inconsistent ink flow on the black permanent ink side.

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

Class III — Low RiskOngoing