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 4522145240 of 47,654 recalls

DrugDecember 17, 2012· L. Perrigo Co.

Recalled Item: Prednisone tablets Recalled by L. Perrigo Co. Due to Presence of Foreign...

The Issue: Presence of Foreign Substance(s); Perrigo has been notified of a recall by...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 17, 2012· Animas Corporation

Recalled Item: Animas(R) 2020 Recalled by Animas Corporation Due to Due to an internal...

The Issue: Due to an internal calendar date limit (December 31, 2015) these pumps will...

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

Class III — Low RiskOngoing
Medical DeviceDecember 17, 2012· Mizuho OSI

Recalled Item: Mizuho Orthopedic Table Recalled by Mizuho OSI Due to Possible instability...

The Issue: Possible instability of Orthopedic Table Top. If the epoxy bond fails, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2012· Medacta Usa Inc

Recalled Item: Medacta Quadra Trial Broach size 0 part # 01.10.10.045 Recalled by Medacta...

The Issue: The tip of the Quadra Trial Broach size 0, broke during a surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2012· Intel-GE Care Innovations LLC

Recalled Item: QuietCare-Networked product Recalled by Intel-GE Care Innovations LLC Due to...

The Issue: Care Innovations detected a software anomaly: During the engineering...

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

Class II — Potential Health HazardOngoing
DrugDecember 14, 2012· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Mylan...

The Issue: Superpotent (Multiple Ingredient) Drug: Oversized tablets resulting in...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 13, 2012· Watson Laboratories Inc

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

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

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

Class III — Low RiskOngoing
Refund
FoodDecember 13, 2012· Ocean Beauty Seafoods, LLC

Recalled Item: Cold-smoked salmon in vacuum plastic bags that are partially clear Recalled...

The Issue: Ocean Beauty Seafood's sample was found positive for Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 13, 2012· Ocean Beauty Seafoods, LLC

Recalled Item: Cold-smoked salmon in vacuum plastic that are partially clear and Recalled...

The Issue: Ocean Beauty Seafood's sample was found positive for Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 13, 2012· Natural Organics

Recalled Item: Nature's Plus GLUTEN Free SPIRU-TEIN HIGH PROTEIN ENERGY MEAL Recalled by...

The Issue: One lot of 1.2 oz. packets of Spiru-tein High Protein Energy Meal, S'mores...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 13, 2012· Sr Instruments Inc

Recalled Item: SR Instruments FG3105 Patient Scales Used on various Joerns Healthcare...

The Issue: SR Instruments Inc. is implementing a field correction for the Joerns...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2012· Medical Components, Inc dba MedComp

Recalled Item: Recalled by Medical Components, Inc dba MedComp Due to The affected product...

The Issue: The affected product was packaged with the incorrect introducer needle. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2012· Ortho-Clinical Diagnostics

Recalled Item: Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption...

The Issue: Some VITROS¿ Chemistry Products Vapor Adsorption Cartridge CAT No. 6800100...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2012· Philips Healthcare Inc.

Recalled Item: Juno DRF Recalled by Philips Healthcare Inc. Due to Values of fluoroscopy...

The Issue: Values of fluoroscopy time, Air Kerma Rate and Cumulated Air Kerma may not...

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

Class II — Potential Health HazardOngoing
DrugDecember 12, 2012· Schering-Plough Products, LLC

Recalled Item: Temodar (temozolomide) Capsule Recalled by Schering-Plough Products, LLC Due...

The Issue: Failed Impurities/Degradation Specifications: The recall is being initiated...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2012· Boehringer Ingelheim Roxane Inc

Recalled Item: Perindopril Erbumine Tablets Recalled by Boehringer Ingelheim Roxane Inc Due...

The Issue: Impurities/Degradation Products: Out of Specification results found for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 12, 2012· Abbott Laboratories

Recalled Item: Abbott Laboratories Recalled by Abbott Laboratories Due to The Architect...

The Issue: The Architect 25-OH Vitamin D assay has the potential to generate falsely...

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

Class II — Potential Health HazardOngoing
FoodDecember 11, 2012· Whole Foods Market

Recalled Item: Natures Path Hemp Plus Granola sold in bulk bins at Whole Foods PLU 8106...

The Issue: The product has the potential to contain undeclared almond slices.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 11, 2012· Toshiba American Medical Systems Inc

Recalled Item: Aplio 500/400/300 Diagnostic Ultrasound System (TUS-500/400/300). Device...

The Issue: Toshiba Medical Systems has received reports of startup issues with the...

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

Class II — Potential Health HazardOngoing
DrugDecember 10, 2012· Brower Enterprises Inc

Recalled Item: WOW Recalled by Brower Enterprises Inc Due to Undeclared Drug

The Issue: Marketed without an Approved NDA/ANDA: Brower Enterprises Inc., is recalling...

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

Class I — Serious Health HazardOngoing
Refund