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. 2,725 recalls have been distributed to Indiana in the last 12 months.
Showing 9721–9740 of 29,228 recalls
Recalled Item: Surgistool-intended to support a healthcare professional during surgical...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric MedSurg Bed FL23 - AC-powered adjustable hospital bed with Recalled...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruRize Clinical Chair - support structure that places human occupants...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isolibrium Support Surface - support surface assists in the prevention...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime TC-transport chair intended for medical purposes to assist a Recalled...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus Recalled by Encore...
The Issue: Packaging mixup; There is a potential that packaging identified as 12mm knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus Recalled by Encore...
The Issue: Packaging mixup; There is a potential that packaging identified as 12mm knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT....
The Issue: The HAT trial contains a retaining ring that has shown the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: novaplus Recalled by Medical Action Industries, Inc. 306 Due to There is a...
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...
The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of...
The Issue: Standard packed within NEFA kit has been assigned incorrectly. Calibrating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit...
The Issue: A risk exists during impacting of the acetabular cup into the bone the plugs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog...
The Issue: Due to a component failure, ventilators may unexpectedly shut down or have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...
The Issue: Elevated rates of false negative results may occur when using blood culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098 Recalled by...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004 Recalled by...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.