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. 2,560 recalls have been distributed to Indiana in the last 12 months.
Showing 23981–24000 of 53,528 recalls
Recalled Item: Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg...
The Issue: Edi Catheter labeled with wrong expiry date on single pack EDI catheter boxes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...
The Issue: Potential for sample fluid to be dispensed to an incorrect position on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON...
The Issue: Advisory issued not to disable or bypass the AMP function. Disabling or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnSight 3D Extremity System- X-Ray Recalled by Carestream Health, Inc. Due...
The Issue: When the user performs the re-assignment of a parent / companion pair, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neomem Resorbable Collagen Membrane Recalled by Collagen Matrix, Inc. Due to...
The Issue: Product was packaged in the wrong box; may have been placed inside a Neomem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIR Technology Anterior Array Recalled by GE Healthcare, LLC Due to The...
The Issue: The outer seam of the coil, closest to the system cable, may separate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performance Series Sagittal Blade Recalled by Stryker Instruments Div. of...
The Issue: During manufacture, packaging materials for a small portion of the lot may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walgreens Probiotic 12.5 Billion Active Cultures Recalled by Merical, LLC...
The Issue: Incorrect probiotic strain used in formulation which did not match product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gavilyte-N Recalled by LUPIN SOMERSET Due to Labeling Not Elsewhere...
The Issue: Labeling Not Elsewhere Classified; orange and cherry flavor packets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution Recalled by Ingenus Pharmaceuticals Llc...
The Issue: Defective Container: firm discovered samples stored horizontally as well as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IDEAL IMPLANT Structured Breast Implant Recalled by Ideal Implant...
The Issue: The implants were deflating due to a piece of silicone disrupting the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albumin BCP Product Usage: ALBP is an in vitro test Recalled by Roche...
The Issue: The reagent lot is exhibiting calibration failures, QC imprecision, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Continuous...
The Issue: Continuous operation at very high tube output may result in increased wear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 801 immunoassay analyzer Recalled by Roche Diagnostics Corporation...
The Issue: The firm has confirmed complaints regarding signal drops on the cobas e 801...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat...
The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...
The Issue: There is a potential for loss of the x-ray imaging function when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova IGS 6 Recalled by GE Healthcare, LLC Due to There is a potential for...
The Issue: There is a potential for loss of the x-ray imaging function when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat...
The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...
The Issue: There is a potential for loss of the x-ray imaging function when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.