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. 2,462 recalls have been distributed to Indiana in the last 12 months.
Showing 43261–43280 of 53,528 recalls
Recalled Item: Contact Detach 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: Silhouette Paradigm 13mm 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: 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: 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 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: 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: 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: 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: Synthes Small Electric Drive (SED) Recalled by Synthes (USA) Products LLC...
The Issue: The device may operate solely in reverse mode, not operate in reverse mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CHEMISTRY PRODUCTS TRIG Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Potential for biased results using the specific lot of VITROS CHEMISTRY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate...
The Issue: AMO has received complaints where the finger grip dislodged while depressing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED PEDIATRIC R2 Multifunction Electrodes Recalled by ConMed Corporation...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.