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. 1,138 recalls have been distributed to Indiana in the last 12 months.
Showing 4101–4120 of 29,228 recalls
Recalled Item: DAC 044 115cm Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Anti-TG Ab Catalog # L2KTG6 (600 Tests) Recalled by Siemens...
The Issue: The potential for falsely elevated patient sample results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Anti-TG Ab Catalog # L2KTG2 (200 Tests) Recalled by Siemens...
The Issue: The potential for falsely elevated patient sample results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro .014"guide wire Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURGIFOAM" Absorbable Gelatin Powder Kit Recalled by Ethicon, Inc. Due to...
The Issue: Some applicator tips from these lots had open seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo NXT ProVue 3 x 32 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System with Well. Intended to be Recalled by...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preview Strep A Recalled by Wondfo USA Co Ltd Due to Wondfo USA has...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T with Evolution Upgrade 1.5T - Magnetic Resonance (MR) Recalled...
The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE Recalled by MEDLINE...
The Issue: It has been identified that testing documentation does not support that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarity and Clarity Diagnostics LLC Recalled by Wondfo USA Co Ltd Due to...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptococcal A rapid test kits Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T with Evolution Upgrade 3.0T - - Magnetic Resonance Recalled by...
The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System with Well and 2 inch Recalled by Mirion...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptococcal A rapid test kits Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...
The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Independent Medical Co-op Inc. Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX...
The Issue: Capacitors in certain Prucka 3 Amplifiers used with CardioLab / ComboLab...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.