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. 2,667 recalls have been distributed to Indiana in the last 12 months.
Showing 14461–14480 of 53,528 recalls
Recalled Item: Regard Recalled by ROi CPS LLC Due to Kits lacks rubber latex warning label.
The Issue: Kits lacks rubber latex warning label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls Recalled by MEDLINE...
The Issue: Affected product was shipped from the warehouse at room temperature instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Recalled by...
The Issue: Due to: 1) Manufacturing issue that result in inaccurate force measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: activforce 2 package labeling: Model: Activ5-M R 201-200563 Recalled by...
The Issue: Due to: 1) Manufacturing issue that result in inaccurate force measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moxifloxacin Recalled by Denver Solutions, LLC DBA Leiters Health Due to...
The Issue: Labeling: Label Mix-up: Vials labeled as moxifloxacin 1 mg/mL may actually...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Giant Eagle Diced Green Peppers Recalled by Giant Eagle, Inc. Due to Giant...
The Issue: Giant Eagle, Inc., Pittsburgh, PA has initiated a recall of Giant Eagle...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Krispy Kreme DOUGHNUT Bites ORIGINAL GLAZED 5 1.6 OZ (45g) Recalled by...
The Issue: The firm was notified by customers that the product contained metal fragments
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medichoice Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmers w/strap Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heel Snuggler Recalled by Philips North America Llc Due to After the device...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Proton Therapy...
The Issue: Proton Therapy System (PTS) software can be started in the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infa-Therm Transport Mattress Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Recalled by Philips North America Llc Due to Due to a...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Radiotherapy System - System Label: "*** by Medical, Inc. Due to Due...
The Issue: Due to dose discrepancy when delivering a plan to a patient in a Non-HFS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBB-06 Hemodialysis Delivery System Recalled by Nikkiso Ltd - Shizuoka Plant...
The Issue: Device lacks premarket approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Pro Tibial Preparation Tray Recalled by Howmedica Osteonics Corp....
The Issue: Triathlon Pro Tibial Preparation Tray may have been kitted with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Old Spice Recalled by The Procter & Gamble Company Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Old Spice Recalled by The Procter & Gamble Company Due to Chemical...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.