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 3946139480 of 47,654 recalls

Medical DeviceSeptember 17, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...

The Issue: Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to...

The Issue: Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Multi-Function Electrodes (MFE) Part Number: 8900-4012...

The Issue: Product sterility is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m)...

The Issue: Product sterility is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Multi-Function Electrodes (MFE) Single. Part number:...

The Issue: Product sterility is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Baxter Healthcare Corp

Recalled Item: Baxter 2B8011 Empty INTRA VIA Container with PVC Ports Recalled by Baxter...

The Issue: Particulate matter found inside the fluid path.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m)...

The Issue: Product sterility is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Baxter Healthcare Corp

Recalled Item: Baxter 2B8013 Empty INTRA VIA Container with PVC Ports (Sterile Recalled by...

The Issue: Particulate matter found inside the fluid path.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Lumbar Drainage Catheter Kit II with EDS 3 (External Recalled by...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman EDS 3 Drainage System with Ventricular Catheter (External Drainage...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

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

Recalled Item: Siemens ADVIA Centaur¿ Systems HBc Total (HBcT) Recalled by Siemens...

The Issue: Increased imprecision and positive bias is observed with patient samples and...

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

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

Recalled Item: ADVIA Centaur¿¿ Systems HBc Total (HBcT) Kit. For In Vitro Recalled by...

The Issue: Increased imprecision and positive bias is observed with patient samples and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Primus Medical LLC

Recalled Item: AC Powered adjustable bed frame. AC powered adjustable bed frame Recalled by...

The Issue: Firm received several complaints that the head deck actuator bracket had...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman EDS 3 Drainage System (no Ventricular Catheter) (External Drainage...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 15, 2014· Astellas Pharma US Inc

Recalled Item: Tarceva (erlotinib) Tablets Recalled by Astellas Pharma US Inc Due to Failed...

The Issue: Failed Dissolution Specifications: The product did not meet the acceptance...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2014· AbbVie Inc

Recalled Item: CREON (pancrelipase) Delayed-Release Capsules Recalled by AbbVie Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon 13000.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: TOPIRAMATE Tablets 200 mg Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign Tablets: Presence of topiramate 100 mg tablets comingled...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2014· Gel Spice Co, Inc.

Recalled Item: Fresh Finds ground black pepper Net Wt. 3.53 oz (100g) Recalled by Gel Spice...

The Issue: Fresh Finds Black Pepper may contain Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 14, 2014· Invivo Corporation

Recalled Item: Philips Expression Information Portal (IP5) Model 865471. The IP5 is...

The Issue: Frozen Display Numerics and Disabled Menu Keys after extended run time. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer. The Roche...

The Issue: The default for normal values are inconsistent between cobas b 221 and other...

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

Class III — Low RiskOngoing