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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,366 in last 12 months

Showing 4542145440 of 47,654 recalls

Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 9, 2012· Frito Lay, Inc

Recalled Item: Grandma's Peanut Butter Mini Sandwich Creme Cookies Recalled by Frito Lay,...

The Issue: The firm is recalling GRANDMA'S Peanut Butter Sandwich Creme cookies and...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 9, 2012· Frito Lay, Inc

Recalled Item: Grandma's Peanut Butter Sandwich Creme Cookies Recalled by Frito Lay, Inc...

The Issue: The firm is recalling GRANDMA'S Peanut Butter Sandwich Creme cookies and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 9, 2012· Cooper Vision Caribbean Corp.

Recalled Item: AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses...

The Issue: The lenses exceeded the acceptance limit for silicone oil residual.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...

The Issue: GE Healthcare became aware of a potential issue associated with the LOGIQ e...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· Medtronic Neuromodulation

Recalled Item: SynchroMed EL Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 9, 2012· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 9, 2012· Philips Healthcare Inc.

Recalled Item: Philips IntelliVue Information Center/Client and Philips IntelliVue...

The Issue: Internal audio cable may have diminished retention force due to damaged...

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

Class II — Potential Health HazardOngoing
DrugNovember 8, 2012· Hospira Inc.

Recalled Item: Carboplatin Injection Recalled by Hospira Inc. Due to Crystallization:...

The Issue: Crystallization: Product is being recalled due to visible particulates...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 8, 2012· Hospira Inc.

Recalled Item: Carboplatin Injection Recalled by Hospira Inc. Due to Crystallization:...

The Issue: Crystallization: Product is being recalled due to visible particulates...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 8, 2012· Procter & Gamble Co

Recalled Item: Vicks NyQuil Cold & Flu Recalled by Procter & Gamble Co Due to Labeling...

The Issue: Labeling Illegible: Portions of the product labeling in the area of the...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2012· Whole Foods Market

Recalled Item: Whole Foods Market Panettone Chocolate - 26.4 oz Recalled by Whole Foods...

The Issue: The reason for the recall was that a small portion of the Whole Foods Market...

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

Class III — Low RiskOngoing
Refund
FoodNovember 8, 2012· Nestle USA

Recalled Item: Nesquik Chocolate Powder Recalled by Nestle USA Due to Potential Salmonella...

The Issue: Nestle is recalling Nesquik Chocolate Powder because certain lots of its...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 8, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: ShapeMatch Cutting Guides Product Usage: The ShapeMatch Cutting Guides are...

The Issue: With regards to ShapeMatch Cutting Guides using MRI Imaging, Stryker...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2012· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Infinix-i X-Ray System. A radiographic and fluoroscopic x-ray system...

The Issue: Lost and incorrect images. When using the "F-Rec" fluoroscopy image...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2012· Medline Industries Inc

Recalled Item: Medline Angio Drape Pack Radiology-LF Recalled by Medline Industries Inc Due...

The Issue: The non-sterile Waste Bag component in the custom pack was attached to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2012· MOOG Medical Devices Group

Recalled Item: EnteraLite Infinity Enteral Feeding Pump identified with the following list...

The Issue: MOOG Medical Devices Group is conducting a voluntary for a limited set of...

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

Class II — Potential Health HazardOngoing