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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,366 in last 12 months

Showing 4466144680 of 47,654 recalls

Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Shimadzu Medical Systems

Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...

The Issue: The recall was initiated because Shimadzu Corporation has identified a...

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

Class II — Potential Health HazardOngoing
FoodMarch 18, 2013· Magno Humphries Inc

Recalled Item: Ferrous Sulfate Tablets 325 mg Recalled by Magno Humphries Inc Due to The...

The Issue: The firm found minute pieces of blue material identified by their raw...

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

Class III — Low RiskOngoing
Refund
DrugMarch 16, 2013· Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals

Recalled Item: "Well at Wallgreens" Regular Strength Antacid Liquid...

The Issue: Microbial Contamination of Non-Sterile Products: Lot in question had an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Errin (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Balziva(TM) (norethindrone and ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Lessina(R) (Levonorgestrel and ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Junel(TM) Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camila (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa(R) (levonorgestrel/ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2013· Intuitive Surgical, Inc.

Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...

The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Intuitive Surgical, Inc.

Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...

The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· AGFA Corp.

Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...

The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Acist Medical Systems

Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...

The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Vital Images, Inc.

Recalled Item: Vitrea¿ CT Brain Perfusion made available in various configurations under...

The Issue: Vital Images, Inc. (Vital Images) received one report about potential user...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· MCKESSON TECHNOLOGIES INC.

Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...

The Issue: There was an occurrence where the patient case data did not match the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
DrugMarch 14, 2013· Med Prep Consulting, Inc.

Recalled Item: Magnesium Sulfate 2 grams in Dextrose 5% for Injection Recalled by Med Prep...

The Issue: Non-Sterility; mold contamination

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camrese(TM) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...

The Issue: Failed Impurity/Degradation Specifications; an impurity identified as...

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

Class III — Low RiskOngoing
Refund