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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,360 in last 12 months

Showing 4658146600 of 47,654 recalls

Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 1 Gold Rover (120 Vand 230V ) Waste Management Recalled by Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2012· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Slice CT Scanner System is a computed Tomography X-ray...

The Issue: One of the four screws that secure the Oil-accumulator to the X-Ray Tube...

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

Class II — Potential Health HazardOngoing
DrugJune 7, 2012· Fougera Pharmaceuticals, Inc.

Recalled Item: Erythromycin Topical Solution USP Recalled by Fougera Pharmaceuticals, Inc....

The Issue: Chemical Contamination: This product is being recalled because trace amounts...

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

Class III — Low RiskOngoing
Refund
FoodJune 7, 2012· SUNFRESH NATURAL LLC.

Recalled Item: SunFresh Natural Pitted Prunes Net wt. 6 oz. Distributed by: Recalled by...

The Issue: Prunes contained Rhodamine B45170 as unapproved color. The product also...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 7, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Stratus(R) CS Acute Care(TM) D-dimer Calibrator (DDM CalPak) lots...

The Issue: Siemens has confirmed that the Stratus(R) CS Acute Care(TM) D-Dimer CalPak...

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

Class III — Low RiskOngoing
Medical DeviceJune 7, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens syngo(R) Lab Data Manager. The syngo(R) Lab Data Manager Recalled by...

The Issue: The recalling firm has discovered that when using a Sysmex(R) CA-7000 or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: EasyLink(TM) Informatics System Recalled by Siemens Healthcare Diagnostics,...

The Issue: There is a potential for the EasyLink system to display and transmit to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2012· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Single Shot Epidural Trays Recalled by Integra LifeSciences Corp. d.b.a....

The Issue: Integra LifeSciences is recalling one lot of Single Shot Epidural Trays as...

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

Class III — Low RiskOngoing
Medical DeviceJune 7, 2012· Arrow International Inc

Recalled Item: Arrow International Recalled by Arrow International Inc Due to Arrow is...

The Issue: Arrow is recalling the product due to the possibility of voids in the...

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

Class II — Potential Health HazardOngoing
DrugJune 6, 2012· Meridian Medical Technologies a Pfizer Company

Recalled Item: Diazepam Injection Recalled by Meridian Medical Technologies a Pfizer...

The Issue: Impurities/Degradation Products: High Out of Specification levels for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo.plaza radiological image processing system. Recalled by...

The Issue: Siemens became aware of an unintended behavior when using syngo.plaza. In...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2012· Zoe Medical Incorporated

Recalled Item: Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3...

The Issue: Unit fails to power up, resulting in an equipment alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2012· Sendx Medical Inc

Recalled Item: ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with Recalled by Sendx...

The Issue: The firm recalled because the glucose measurements from a patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Rigid Suction Wand Recalled by Edwards Lifesciences,...

The Issue: Edwards is recalling Suction Wand models SPC2081 and S033 because the...

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

Class II — Potential Health HazardOngoing
DrugJune 5, 2012· Bristol-myers Squibb Company

Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...

The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2012· Bristol-myers Squibb Company

Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...

The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2012· Watson Laboratories Inc

Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets Recalled by Watson...

The Issue: Impurities/Degradation Products: High Out-of-specification results were...

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

Class III — Low RiskOngoing
Refund
DrugJune 5, 2012· JHP Pharmaceuticals, LLC

Recalled Item: Pitocin (Oxytocin Injection Recalled by JHP Pharmaceuticals, LLC Due to...

The Issue: Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store...

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

Class III — Low RiskOngoing
Refund
FoodJune 5, 2012· Campbell Soup Supply Co., LLC

Recalled Item: Campbell's Oyster Stew Recalled by Campbell Soup Supply Co., LLC Due to The...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 5, 2012· Zimmer, Inc.

Recalled Item: PathFinder NXT Pivoting Percutaneous Rod Holder This device is an Recalled...

The Issue: Complaints have been reported where, during surgery, the surgeon was unable...

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

Class II — Potential Health HazardOngoing