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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,411 in last 12 months

Showing 3990139920 of 47,654 recalls

Medical DeviceJuly 16, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension EXL Integrated Chemistry System in vitro diagnostic...

The Issue: The Reagent Lid hinge may lose its effectiveness and slowly shift downward...

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

Class II — Potential Health HazardOngoing
DrugJuly 16, 2014· Bio-pharm, Inc.

Recalled Item: Rugby Children's Pain and Fever Acetaminophen Oral Suspension 160 mg/5 mL...

The Issue: Superpotent Drug: Bio-Pharm, Inc. is initiating a recall of one lot of...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2014· Mars Food US

Recalled Item: Uncle Ben's(R) Ready Rice GARDEN VEGETABLE Recalled by Mars Food US Due to...

The Issue: Some pouches were filled with a different product that contains barley, a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2014· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 15, 2014· Vascutek, Ltd.

Recalled Item: Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a Recalled...

The Issue: The cautery that is provided with the Gelweave graft in the box has a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Chemistry Wash (RD701) is an accessory of the Recalled by...

The Issue: Siemens Healthcare Diagnostics has received complaints for the Dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***BURETROL Solution Set***105" (2.7 m) 150 mL Burette***Drip...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***Non-DEHP***BURETROL Solution Set 105" (2.7 m) Recalled by Baxter...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
DrugJuly 14, 2014· Wockhardt Usa Inc.

Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by Wockhardt Usa Inc. Due to...

The Issue: Failed Impurities/Degradation Products: Out of specification levels of the...

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

Class III — Low RiskOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar HCT Tablets (olmesartan medoxomil Recalled by Daiichi Sankyo Pharma...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Azor Tablets (amlodipine and olmesartan medoxomil) 10 mg*/40 mg Recalled by...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar Tablets (olmesartan medoxomil) 40 mg Recalled by Daiichi Sankyo...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Welchol Tablets (colesevelam HCl) 625 mg Recalled by Daiichi Sankyo Pharma...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar Tablets (olmesartan medoxomil) 20 mg Recalled by Daiichi Sankyo...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide)...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/12.5 mg...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/25 mg...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2014· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Presence of Particulate Matter: particulate matter identified as fibers...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 11, 2014· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP MINI-BAG Plus Container Recalled by...

The Issue: Presence of Particulate Matter: particulate matter identified as fibers...

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

Class I — Serious Health HazardOngoing
Refund