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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18461–18480 of 47,654 recalls
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab Start.Kit LT - ceramic Recalled...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - Recalled by...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 C17/5 -ceramic for dental...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Processor Board PCA Replacement Kits 453563478461 Recalled by...
The Issue: Damaged ESD bags used for storing components in Processor PCA Replacement Kits
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.