Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,909 recalls have been distributed to Indiana in the last 12 months.
Showing 27721–27740 of 53,528 recalls
Recalled Item: MultiDiagnostic-Eleva with Flat Detector 708035 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 Eleva with Flat Detector 708037 As...
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: 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: 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: 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: King Arthur Flour Recalled by The King Arthur Flour Company, Inc. Due to...
The Issue: Coconut flour tested positive for Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.