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. 2,445 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,445 in last 12 months

Showing 3274132760 of 47,654 recalls

Medical DeviceApril 20, 2016· Acorn Stairlifts, Inc

Recalled Item: Acorn 130 Stairlift Recalled by Acorn Stairlifts, Inc Due to The design of...

The Issue: The design of the seats did not consistently have the adequate strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2016· Ortho-Clinical Diagnostics

Recalled Item: The VITROS¿ Chemistry Products Calibrator Kit 31 Recalled by Ortho-Clinical...

The Issue: There is an incorrect value (data/calibration mathematics) on ADDs. This...

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

Class III — Low RiskOngoing
Medical DeviceApril 19, 2016· Berchtold Corp.

Recalled Item: Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional Recalled...

The Issue: The Surgical Table Cushion (HybriGel Pads) could potentially contain staples...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2016· Elekta, Inc.

Recalled Item: Radionuclide Radiation Therapy System Product The product is a teletherapy...

The Issue: The latches of the frame adapter can be locked even if the locating pins of...

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2016· VistaPharm, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: Excess lidding material accumulation between the seal...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 18, 2016· Synthes (USA) Products LLC

Recalled Item: 3.2 mm Three-fluted drill bit Recalled by Synthes (USA) Products LLC Due to...

The Issue: The sterile packaging may be compromised. A protective cap is to be secured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2016· Synthes (USA) Products LLC

Recalled Item: 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile...

The Issue: The sterile packaging may be compromised. A protective cap is to be secured...

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

Class II — Potential Health HazardOngoing
FoodApril 15, 2016· FoodState, Inc

Recalled Item: MegaFood Multi for Women 40+ Recalled by FoodState, Inc Due to Multi Vitamin...

The Issue: Multi Vitamin label fails to have required warning statement for iron and...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2016· Health 4 Life, LLC

Recalled Item: Passion 4 Life 30 FL oz. Bottle Recalled by Health 4 Life, LLC Due to...

The Issue: Undeclared whey protein containing the allergens of milk and soy lecithin.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 15, 2016· Merge Healthcare, Inc.

Recalled Item: Merge LIS software. The firm name on the label is Recalled by Merge...

The Issue: There are potential issues with results reporting for certain run-based...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Therapy Knee Wrap Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Frostie Heated Gloves (All sizes) Deep penetrating heat...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing