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. 1,967 recalls have been distributed to Indiana in the last 12 months.
Showing 22121–22140 of 29,228 recalls
Recalled Item: Allura Xper FD10 OR Table Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 15-12 (biplane) Recalled by Philips Electronics North...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 OR Table Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper FD20 Ceiling version only Recalled by Philips...
The Issue: Normally, movement of the C-arc is initially stopped by the motor (holding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...
The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD V4.1 CLI Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (RUO) Recalled by Diagnostic Hybrids, Inc. Due to A...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (CE-IVD) Recalled by Diagnostic Hybrids, Inc. Due...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to A component...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.