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. 1,097 recalls have been distributed to Indiana in the last 12 months.
Showing 16101–16120 of 53,528 recalls
Recalled Item: SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Recalled...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Recalled by...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Recalled...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Recalled...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Recalled...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Recalled by...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Recalled...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system Recalled...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Recalled...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENOSYL DS Recalled by Vero Biotech, LLC Due to Reports received of NO...
The Issue: Reports received of NO measured below desired dose during transition between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with Recalled by Bard...
The Issue: Catheter convenience kits contain the incorrect guidewire. Kits were labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION Posterior Stabilized OXINIUM Femoral Component Recalled by Smith &...
The Issue: The device components experienced a manufacturing process error that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 10cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 5cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ADVIA Chemistry XPT Chemistry System Recalled by Siemens Healthcare...
The Issue: ADVIA Chemistry System and Software Versions (V1.4 SMN 11314625 and V1.4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PremierZEN Platinum 8000 capsule Recalled by Miracle 8989 Due to Marketed...
The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.