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 4314143160 of 47,654 recalls

DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA Balanced Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400 ec Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 28, 2013· Alphatec Spine, Inc.

Recalled Item: Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico Recalled by...

The Issue: The firm initiated this recall of certain lots of Illico Ti Cannulated...

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

Class II — Potential Health HazardOngoing
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's OsteoSheath 4 Enhanced Bone Support Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath 4...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand brand ROASTED SALTED PISTACHIOS Recalled by Priester...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's OsteoSheath Enhanced Bone Support Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand FANCY ROASTED NUTS Recalled by Priester Pecan...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's Fem-Vite Women's Anti-Oxidant Formula Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Fem-Vite was...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand NUTTY FAVORITES ASST Recalled by Priester Pecan...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 27, 2013· Insight Instruments, Inc.

Recalled Item: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25-...

The Issue: The product was registered and distributed as a Class I medical device and...

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

Class II — Potential Health HazardOngoing
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Hospira Inc.

Recalled Item: Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer report of visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Clalis capsules Recalled by Fabscout Entertainment, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Silver Sword capsules Recalled by Fabscout Entertainment, Inc Due to...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers Recalled...

The Issue: Customers complained of a positive bias in patient results on the IMMULITE/...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: ADVIA 120 Hematology Analyzer Recalled by Siemens Healthcare Diagnostics Due...

The Issue: The ADVIA 120 optics cover or hood is located on the very top of the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Mar Cor Purification

Recalled Item: Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model...

The Issue: High inlet water pressure beyond specification and the solenoid valve does...

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

Class II — Potential Health HazardOngoing