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. 2,018 recalls have been distributed to Indiana in the last 12 months.
Showing 15021–15040 of 29,228 recalls
Recalled Item: Maximum Variable Pitch Compression Screw Caddy Recalled by Zimmer Biomet,...
The Issue: There is a potential for silicone shedding during cleaning and sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Variable Pitch Compression Tray Base Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for silicone shedding during cleaning and sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant....
The Issue: The surgical technique is being updated to caution against misuse due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESERVOIR "Y" ADAPTER Recalled by Medtronic Perfusion Systems Due to...
The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Recalled...
The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 4x5 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProtectIV¿ Plus Safety IV Catheter Recalled by Smiths Medical ASD Inc. Due...
The Issue: Certain lots of the Model 306701 ProtectIV¿ Plus Safety IV Catheter may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recalled by Abbott...
The Issue: The device is unable to pair with the mobile app due to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Suture Anchor Recalled by Arthrex, Inc. Due to Potentially lead to...
The Issue: Potentially lead to anchor breakage during insertion,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SP CAL (LIQ) Recalled by Randox Laboratories Ltd. Due to Calibrator value...
The Issue: Calibrator value sheets have been modified for assigned value of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model...
The Issue: HVAD Battery Charger units manufactured with wrong inductors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireSR Recalled by LivaNova USA Inc Due to This...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireHC Model 105 Generator Recalled by LivaNova USA...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2 Recalled by LivaNova USA...
The Issue: This recall is being initiated due to reports that that the therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LivaNova VNS Therapy System Recalled by LivaNova USA Inc Due to Lead...
The Issue: Lead impedance values reported by the affected VNS generator will be higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare 9805 and 9805P Hydraulic Patient Lifts Recalled by Invacare...
The Issue: Invacare has identified via customer complaints, the potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...
The Issue: Labeling error. The product is labeled with an 18 month expiration date,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.