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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,448 in last 12 months

Showing 2388123900 of 27,451 recalls

Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ Congruent Tibial Insert with Screw: SF-CON TIB INS LT Recalled...

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: Natural-Knee¿ N-K II DOMED ALL-POLY PAT Recalled by Zimmer, Inc. Due to A...

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· 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 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· 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 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
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 20, 2014· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter and PENTARAY NAV ECO Catheter...

The Issue: Biosense Webster is recalling the PentaRay Nav Catheter because it has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS TT4 Calibrator For the quantitative measurement of total thyroxine...

The Issue: Total T4 Calibrators and Reagent Packs may have calibration failures or low...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2014· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Flash Blood Glucose Monitors System. Meter made in China Recalled...

The Issue: Abbott Diabetes Care has identified through internal testing and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2014· Medefil Incorporated

Recalled Item: Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes...

The Issue: The bar code that is printed on the Master Carton label does not correspond...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 19, 2014· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Blood Glucose Monitors System. For in vitro diagnostic use...

The Issue: Abbott Diabetes Care has identified through internal testing and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A Recalled...

The Issue: MRx may display a Red X in the Ready For Use (RFU) indicator during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...

The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J...

The Issue: Philips HeartStart MRx Monitor/Defibrillator, when operating on battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...

The Issue: A component of the MRx Processor Board may be susceptible to damage from...

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

Class II — Potential Health HazardOngoing