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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,459 in last 12 months

Showing 2554125560 of 47,654 recalls

Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Recalled by...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Ninepoint Medical Inc.

Recalled Item: NvisionVLE¿ Low-Profile Optical Probe Recalled by Ninepoint Medical Inc. Due...

The Issue: Distal tips of the probes may detach from the probe shaft during use.

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

Class II — Potential Health HazardOngoing
DrugApril 10, 2018· Pharmalucence, Inc.

Recalled Item: Kit for the Preparation of Technetium TC-99M Mebrofenin Recalled by...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...

The Issue: Defective Delivery System: Out of specification for adhesive transfer.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 9, 2018· Cenorin, LLC

Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...

The Issue: There is a supplier quality issue with the terminal blocks which may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Covidien LLC

Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...

The Issue: There is a potential for improper welding of the yellow staple guide to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Covidien LLC

Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...

The Issue: There is a potential for improper welding of the yellow staple guide to the...

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

Class II — Potential Health HazardOngoing
DrugApril 6, 2018· Sandoz Incorporated

Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Sandoz Incorporated...

The Issue: Cross Contamination With Other Products: presence of unrelated ingredients...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: T-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Straight Plate Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: TN Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Box Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM Recalled by Orthofix,...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Y-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: L-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Rival View Kit Locking and Non-Locking Screw D 2.7MM Recalled by Orthofix,...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Lapidus Plate Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: CC Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: MTP Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing