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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.
Showing 11841–11860 of 27,451 recalls
Recalled Item: MEDTRONIC BONE VOID FILLER Recalled by Skeletal Kinetics, Llc Due to Bone...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 2CC INJECT FORMULA. Product Number: 390-0002 Recalled by...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION EX Recalled by Skeletal Kinetics, Llc Due to Bone void filler...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRANIOSCULPT Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cranio/Sculpt C Recalled by Skeletal Kinetics, Llc Due to Potential product...
The Issue: Potential product mix-up. The recalling firm has determined that one unit of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic manual Surgical Instrument handle for Simple Locking Intra...
The Issue: The lot number on the pediatric orthopedic implant driver instrument handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 5CC INJECT FORMULA. REF/UDI: 390-2005/00813845020054 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION RMX 10 CC Injectable. REF/UDI: 390-6002/ /00813845021099 -...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 10CC INJECT FORMULA. REF/UDI: 390-2010/00813845020061 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION RMX Injectable BVF 5CC . REF/UDI: 390-6001/ /00813845021082 -...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001...
The Issue: During Giraffe Shuttle charging, the batteries emit low concentrations of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 3CC IMPACTFORMULA. REF/UDI: 390-2103/00813845020078 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 5CC IMPACTFORMULA. REF/UDI: 390-2105/00813845020085 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator APS Aliquoter Module Recalled by Abbott Laboratories Due to In...
The Issue: In the case of an AQM clot detection error a portion of the distilled water...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 3CC IMPACTFORMULA. REF/UDI: 390-0203/00813845020030 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 10 CC IMPACT FORMULA. REF/UDI: 390-2110/ /00813845021092 -...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.