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. 1,882 recalls have been distributed to Indiana in the last 12 months.
Showing 31941–31960 of 53,528 recalls
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11.5MM Product Number:...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM Product Number:...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIVERSAL FLEX2 BREATHING CIRCUIT Recalled by King Systems Corp. dba Ambu,...
The Issue: Potential for leak test failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040...
The Issue: During patient interventions with the urology table the radiation is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App versions 2.0.0 Recalled by Roche...
The Issue: A program error (bug) in the Bolus Advisor feature, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The...
The Issue: The Pause function on central monitors will not automatically resume when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Oral Suspension Recalled by Akorn Inc Due...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Small Particle Aerosol Generator Model SPAG-2 6000 Series (SPAG-2). The...
The Issue: SPAG-2 unit nebulizers from Lot J0571670RA were tested at Next Breath for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.