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. 2,547 recalls have been distributed to District of Columbia in the last 12 months.
Showing 15701–15720 of 27,451 recalls
Recalled Item: 708033 URODiagnost As a multifunctional universal imaging application system...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva 708036 As a multifunctional universal imaging...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnostic-Eleva with Flat Detector 708038 As a multifunctional...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDim Eleva 708032 As a multifunctional universal imaging application...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire Bullet Tip 2.4 mm Diameter...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length Recalled by Zimmer...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...
The Issue: Use of the product with insufficient lubrication may prolong surgery due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire Bullet Tip 3.0 mm Diameter...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Sentinel Intramedullary Reaming System Guide Wire Bullet Tip 2.4...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smooth Guide Wire Bullet Tip 3.0 mm Diameter Recalled by Zimmer Biomet, Inc....
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...
The Issue: Use of the product with insufficient lubrication may prolong surgery due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...
The Issue: Use of the product with insufficient lubrication may prolong surgery due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.