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. 2,723 recalls have been distributed to Indiana in the last 12 months.
Showing 10321–10340 of 29,228 recalls
Recalled Item: Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack Infant Tubingset Pixie Flow 0 Recalled by Medtronic...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack CP 1/4-1/4 Pediatric Set 1/B (PERFUSION M484901D...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack CP Kinderset 1/4-1/4 MIT Pixie 1/B (PERFUSION Recalled...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Perfusion System (CUSTOM PACK HY10J00R6 ECC SMALL CAR). The Recalled...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Perfusion System (CUSTOM PACK BB7W03R8 CCSM NEON). The Affinity...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Affinity Pixie BP241 Hollow Fiber Oxygenator and Cardiotomy/Venous...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista HDLC - colorimetric method Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coronavirus antigen detection test system - Product Usage: intended for...
The Issue: Two lots of test strips failed QC testing using blank buffer due to false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable cardioverter defibrillators (ICD) with cardiac resynchronization...
The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR...
The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America Llc Due to...
The Issue: Manufacturing failed to follow process steps resulting in the distribution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Ophthalmic Surgical Procedure Packs Recalled by Alcon Research,...
The Issue: Reports have been received concerning mold found on gowns included in custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Feth-R-Kath Catheter Recalled by Epimed International, Inc. Due to Outer...
The Issue: Outer coating of the catheter may deteriorate and result in the coating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velocity Disposable Bipolar Ablators - Product Usage: intended to be...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HNM Disposable Bipolar Ablators - Product Usage: intended to be used for...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Disposable Bipolar Ablators - Product Usage: intended to be Recalled...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia (N) 180 - Drager Breathing Circuits/Anesthesia Sets...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma)...
The Issue: Due to two (2) issues: 1) The firm distributed COVID-19 Rapid Test Cassettes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.