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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,411 in last 12 months

Showing 4114141160 of 47,654 recalls

Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Apollo" Knee System: PS TIB INS SZ0/16MM APOLL PS TIB Recalled by Zimmer,...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Apollo" Knee System: APOLLO PATELLA SZ0 28MM R Recalled by Zimmer, Inc. Due...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· Allesee Orthodontic Appliances

Recalled Item: AOA Distalizer Lock Nut Screw Recalled by Allesee Orthodontic Appliances Due...

The Issue: The Lock Nut component of the Jet appliances may be missing the screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: R S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: R Recalled by DePuy Orthopaedics, Inc. Due to DePuy Orthopaedics has...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L Recalled by DePuy Orthopaedics, Inc. Due to DePuy Orthopaedics has...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: RS-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2014· Medical Information Technology, Inc.

Recalled Item: MEDITECH Microbiology Recalled by Medical Information Technology, Inc. Due...

The Issue: Potential for erroneous result reporting.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2014· DeRoyal Industries Inc

Recalled Item: DeRoyal(R) LIMB HOLDERS Recalled by DeRoyal Industries Inc Due to Moldy...

The Issue: Moldy smell in product

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

Class II — Potential Health HazardOngoing
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette Lozenge and NicoDerm CQ Recalled by GlaxoSmithKline Consumer...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette Lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini Recalled by GlaxoSmithKline...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini Recalled by GlaxoSmithKline...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund