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 4050140520 of 47,654 recalls

Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Face Pack FJG Recalled by Customed, Inc Due to Customed has determined that...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROTOMY PACK - CUSTOMED- (1) BAG SUTURE FLORAL (2) TOWEL Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LITHOTOMY PACK CONTENTS: (2) TOWELS ABSORBENT 15" X 20" (2) Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: FEMORAL ANGIOGRAPHY PACK - (1) TABLE COVER REINFORCED 50" X Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROTOMY PACK Ill (4) CUSTOMED CONTENT: (4) TOWEL ABSORBENT 15" Recalled...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Tummy Tuck and Liposuction Pack Recalled by Customed, Inc Due to Customed...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: O.R. TOWELS- CUSTOMED- (6) TOWELS CLOTH HUCK BLUE ( I) Recalled by Customed,...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: 0.B. PACK - - (1) TABLE COVER 44" x 90" Recalled by Customed, Inc Due to...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ORTHOPEDIC PACK I (2) CUSTOMED Recalled by Customed, Inc Due to Customed has...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo Lab Data Manager Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: Certain configuration parameters may cause the ranges to not hold results as...

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

Class II — Potential Health HazardOngoing
DrugMay 20, 2014· West-Ward Pharmaceutical Corp.

Recalled Item: Isoniazid Tablets Recalled by West-Ward Pharmaceutical Corp. Due to Failed...

The Issue: Failed Dissolution Specifications: Stability lots cannot support dissolution...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Integra LifeSciences Corp.

Recalled Item: Accell Evo3C Demineralized Bone Matrix Recalled by Integra LifeSciences...

The Issue: This lot of Accell Evo3C Demineralized Bone Matrix, 5cc was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: VerSys¿ Hip System Recalled by Zimmer, Inc. Due to During routine...

The Issue: During routine inspection, beaded hip stem forgings received from supplier...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing