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. 2,734 recalls have been distributed to Indiana in the last 12 months.
Showing 6561–6580 of 29,228 recalls
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165CM 5/BX- Intended for...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230 CM 10/BX- Intended Recalled...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230CM 5/BX- Intended for...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE THERAHONEY GEL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline issued a recall on TheraHoney Wound Gel due to the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to Device...
The Issue: Device may experience malfunctions due to misalignment of the check valve in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TREO ABDOMINAL STENT-GRAFT SYSTEM (TREO) consists of four types of...
The Issue: Potential for the incorrect size stent-graft than the printed carton label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGACY SMARTBASE Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Non-engaging abutments were distributed without FDA clearance; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy...
The Issue: The inner needle of the Sertera device is either detaching or discharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Sign Sensor 2 Recalled by SenTec AG Due to The sensors may experience an...
The Issue: The sensors may experience an out-of-box failure because after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 EV300 Recalled by Philips Respironics, Inc. Due to...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B Recalled by...
The Issue: IFU- Instructions for Use (IFU) package insert and both the IFU packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Environmental...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: The Trilogy Evo Universal ventilator provides continuous or intermittent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 and LifeVent EVO2 Recalled by Philips Respironics, Inc. Due...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel multiplexed nucleic acid real-time...
The Issue: Faulty cartridges in the lot could result in false test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelli-C Recalled by NRT X-RAY A/S Due to There is a potential that the...
The Issue: There is a potential that the drive shaft in the detector up/down (IDE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.