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. 2,741 recalls have been distributed to Indiana in the last 12 months.
Showing 5701–5720 of 29,228 recalls
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CellQuicken Analyzer (Smart-Watch and Software) Recalled by RoyalVibe Health...
The Issue: Ultrasound devices were not authorized, cleared, or approved by FDA, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citrine Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4500MD Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API3200MD Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citrine QTRAP Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box as labeled: Regard Recalled by CooperSurgical, Inc. Due to Incorrect...
The Issue: Incorrect component descriptions within the "Contents" section on the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates:...
The Issue: Potential for baseplate peripheral holes to be out of specification due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to...
The Issue: Device is breaking while in use, potential for patients to require a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to There is...
The Issue: There is the potential that the safety shield may not properly engage on IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem P Recalled by TECHNO-PATH MANUFACTURING LTD. Due to Technopath...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem S Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM Recalled by...
The Issue: Peripheral coil system detachable has a potential of unsealed pouch packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Medical Products stored on pallets Recalled by Inmar Supply Chain...
The Issue: Various medical devices potentially exposed to rodent and rodent activity....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Full screen error message may occur on patient monitors with affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cinchlock SS Knotless Anchor Inserter Recalled by Stryker Corporation Due to...
The Issue: Expired Product distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical Portex Bivona Pediatric Tracheostomy Tube Recalled by Smiths...
The Issue: The unit box is labeled with an incorrect expiration date (the manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REVERSE PROSTHESIS SHOULDER SYSTEM Recalled by Encore Medical, LP Due to...
The Issue: Reverse shoulder prosthesis package that should contain 5mmx30 screws could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.