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 3841–3860 of 53,528 recalls
Recalled Item: Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS Recalled...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) NASAL PACK Recalled by...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) ENDOSCOPIC SKULL BASE...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) FREE FLAP Recalled by...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) CRANI Recalled by...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Merlin PCS 3650 programmer Model 3330 The Merlin PCS Recalled by Abbott...
The Issue: Due to a programmer software anomaly, during finalizing of the leadless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 3D Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc Due...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9900 Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mama Mancini s Stuffed Shells with Sauce and Mozzarella Cheese Recalled by...
The Issue: Products have the potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.