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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,395 in last 12 months

Showing 4226142280 of 47,654 recalls

Medical DeviceOctober 2, 2013· Intuitive Surgical, Inc.

Recalled Item: Single Site Curved Needed Driver Intuitive Surgical Recalled by Intuitive...

The Issue: A limited number of FDA-cleared instruments for da Vinci Single Site use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2013· Intuitive Surgical, Inc.

Recalled Item: Single Site Bipolar Maryland Forceps Intuitive Surgical Recalled by...

The Issue: A limited number of FDA-cleared instruments for da Vinci Single Site use,...

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

Class II — Potential Health HazardOngoing
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Everything Net Wt. 9.6 oz (272 Recalled by R.A.B....

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

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

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Onion Net Wt. 9.6 oz (272 Recalled by R.A.B. Food...

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

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

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Unsalted Net Wt. 9.6 oz (272 Recalled by R.A.B. Food...

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

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

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Original Net Wt. 9.6 oz (272 Recalled by R.A.B. Food...

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

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

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Garlic Net Wt. 9.6 oz (272 Recalled by R.A.B. Food...

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

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

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· Grato Inc.

Recalled Item: Apotheca Energique Gastrozyme Recalled by Grato Inc. Due to The products may...

The Issue: The products may contain chloramphenicol.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 1, 2013· Toshiba American Medical Systems Inc

Recalled Item: TSX-101A Aquilion 32/64 ONE Computed Tomography X-Ray System Recalled by...

The Issue: Toshiba intitiated this recall because their investigation revealed that due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe¿ and Panda¿ iRes Infant Warmer Product Recalled by...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe and Panda Bag and Mask Resuscitation System Recalled...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe Warmer Recalled by GE Healthcare, LLC Due to Oxygen...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker...

The Issue: Stryker received a report from the field indicating that a 5.5 mm Cancellous...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2013· Helix Medical LLC

Recalled Item: Blom-Singer Adjustable Tracheostoma Valve II Models: BE8025H and BE8025H-R3...

The Issue: InHealth Technologies (IHT) is recalling the Blom-Singer Adjustable...

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

Class III — Low RiskOngoing
DrugSeptember 30, 2013· G & W Laboratories Inc

Recalled Item: G & W Fluocinolone Acetonide Cream USP 0.025% Recalled by G & W Laboratories...

The Issue: Failed Content Uniformity Specifications; at the 18 month time point.

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 30, 2013· Merit Medical Systems, Inc.

Recalled Item: Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine...

The Issue: Custom Procedural Trays/Kits contain 1% Lidocaine HCl injection which were...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Recalled...

The Issue: Stryker has received complaints associated with cracks and/or fracture of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Rim Impactor Tip Product Usage: Used for MDM Recalled...

The Issue: Stryker has received complaints associated with cracks and/or fracture of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Zero-P VA Implant 7 MM Height Parallel Sterile The Recalled by...

The Issue: A potential non conformance was identified with the Zero-P VA plate where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...

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

Class II — Potential Health HazardOngoing