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. 1,955 recalls have been distributed to Indiana in the last 12 months.
Showing 24021–24040 of 29,228 recalls
Recalled Item: ADULT/CHILD Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b)...
The Issue: A design deficiency was discovered whereby the Drill/Awl Sleeve and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT/CHILD Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSA Medical truFreeze System Recalled by CSA Medical Due to An increase in...
The Issue: An increase in complaint trending for a loss of audible sound associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Nerve Block Component Recalled by Arrow International Inc Due to Arrow...
The Issue: Arrow is recalling certain lots of the Continuous Nerve Block Component,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Cabinet X-ray systems Recalled by GE Inspection Technologies, LP Due to...
The Issue: GE discovered these cabinet x-ray systems' potential failure to comply with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized...
The Issue: Complaints have indicated that the ATTUNE INTUITION Impaction Handle lever...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3i T3 Non-Platform Switched Tapered Implant Rx Only Recalled by Biomet 3i,...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled...
The Issue: Unintended treatment termination could result from a keypad malfunction in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSEOTITE Certain 2 Implant Rx only Recalled by Biomet 3i, LLC Due to...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Integra Licox Recon Tissue...
The Issue: Due to a complaint, it was determined that multiple lots of Licox catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSEOTITE Tapered Certain Implant Rx Only Recalled by Biomet 3i, LLC Due to...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusion Set Recalled by Unomedical As Due to Tubing detachment
The Issue: Tubing detachment
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureT G29 6mm Recalled by Unomedical As Due to Tubing detachment
The Issue: Tubing detachment
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comfort 5+5 Pack w/110cm Tube & 17mm Cann. UPC# 3-89110-14147-7 Recalled by...
The Issue: Tubing detachment
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC TenderLink 13/30 10 pcs Recalled by Unomedical As Due to Tubing detachment
The Issue: Tubing detachment
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.