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. 2,752 recalls have been distributed to Indiana in the last 12 months.
Showing 4181–4200 of 29,228 recalls
Recalled Item: Total Knee Arthroplasty (TKA) 2 Recalled by Stryker Orthopaedics Due to...
The Issue: Application software intended to be deployed on Mako 3.0, part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower Recalled by CareFusion...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in...
The Issue: Potential damage to the cartridge can result in poor staple formation and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower Recalled by CareFusion 303,...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system....
The Issue: The firm identified that the measured patient leakage current in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT - Computed Tomography X-Ray System intended to produce Recalled...
The Issue: Metal mounting box on the rotating scanner on rotor (heat change box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT - Computed Tomography X-Ray System intended to produce Recalled...
The Issue: Metal mounting box on the rotating scanner on rotor (heat change box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTUS 2.8 TriLock Screw 22mm Recalled by Medartis Inc. Due to Screw is 16mm...
The Issue: Screw is 16mm long instead of 22mm long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial mobile application Recalled by Securitas Healthcare LLC Due to The...
The Issue: The Arial Mobile Application utilizing Apple iOS 17.4 and iOS 17.5 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FDR Visionary Suite - Intended to generate digital or conventional Recalled...
The Issue: Bolts on the CH-200 tube may rupture due to fatigue failure, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Noblus AC Adapter used with the Noblus Ultrasound Imaging System Recalled by...
The Issue: AC adapters of Noblus can heat up, and cause smoke in the worst case, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica HistoCore PEGASUS Tissue Processor Recalled by LEICA BIOSYSTEMS...
The Issue: Poorly processed and/or damaged biopsy tissue specimens on the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HealthCare CRITIKON ONE-CUF blood pressure cuffs Recalled by GE Medical...
The Issue: Use of the blood pressure cuffs could result in inaccurate non-invasive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...
The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...
The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Free T3 Calibrators-IVD are for use with...
The Issue: Free T3 Calibrators used with T3 Reagent Packs may produce positively biased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum IQ Infusion pump Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential for cracks on the mount of the front panel of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Free T3 Reagent Pack-IVD is for the...
The Issue: T3 Reagent Packs used with Free T3 Calibrators may produce positively biased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) NEPHROLOGY PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.