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. 2,359 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,359 in last 12 months

Showing 4752147540 of 47,654 recalls

Medical DeviceAugust 18, 2010· Tosoh Bioscience Inc

Recalled Item: G7 HPLC. Used as an aid in the detection and Recalled by Tosoh Bioscience...

The Issue: The Beta-thalessemia Mode of the G7 Analyzer-Beta Thalassemia Mode is an...

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

Class III — Low RiskOngoing
Medical DeviceAugust 11, 2010· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: DPM 6/7 Patient Monitor Manufactured in China for : Mindray DS USA Recalled...

The Issue: There is an issue with the DPM 6 and DPM 7 monitors where the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2010· Breg Inc, An Orthofix Company

Recalled Item: Polar Dressing Recalled by Breg Inc, An Orthofix Company Due to Mislabeling

The Issue: This recall has been initiated due to confirmation that the Polar Dressing,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2010· Clinical Diagnostic Solutions

Recalled Item: Boule Con Diff US Tri Pack Recalled by Clinical Diagnostic Solutions Due to...

The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled the Boule Con...

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

Class III — Low RiskOngoing
Medical DeviceAugust 4, 2010· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Hematology Control 9 vials. For in vitro diagnostic Recalled...

The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled the Boule Con...

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

Class III — Low RiskOngoing
Medical DeviceJuly 29, 2010· Technidata S.A.

Recalled Item: TD-Synergy. Laboratory Information System. Recalled by Technidata S.A. Due...

The Issue: Technidata has discovered that using the F8 key in the ERM session to add a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran Minicat00158 Recalled by Xoran Technologies, Inc. Due to The MiniCAT...

The Issue: The MiniCAT CT Scanners subject to this notification failed to meet Xoran's...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran Minicat00202 Recalled by Xoran Technologies, Inc. Due to The MiniCAT...

The Issue: The MiniCAT CT Scanners subject to this notification failed to meet Xoran's...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran MiniCAT CT Scanner Recalled by Xoran Technologies, Inc. Due to A...

The Issue: A description of the defect in the product or the manner in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran MiniCAT00202 Recalled by Xoran Technologies, Inc. Due to The MiniCAT...

The Issue: The MiniCAT CT Scanners subject to this notification failed to meet Xoran's...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran Mini CT Scanner Recalled by Xoran Technologies, Inc. Due to A...

The Issue: A description of the defect in the product or the manner in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2010· Kimberly-Clark Corporation

Recalled Item: Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark Recalled by...

The Issue: The placement guidewire diameter is too large and does not pass-through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2010· Kimberly-Clark Corporation

Recalled Item: Kimberly-Clark MIC PEG Kit - Pull Type The Kimberly-Clark MIC Recalled by...

The Issue: The placement guidewire diameter is too large and does not pass-through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle 2.75"...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle 4.0"...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Staight Microsurgical Needle 3cm...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing