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. 2,455 recalls have been distributed to Indiana in the last 12 months.
Showing 45261–45280 of 53,528 recalls
Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sevoflurane Recalled by Piramal Critical Care, Inc. Due to Failed pH...
The Issue: Failed pH Specifications: product was too acidic.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mercaptopurine Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azathioprine Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kit 8551/856X (includes Models 8561 Recalled by Medtronic Neuromodulation...
The Issue: Some kits in the affected lots may contain an extension tubing set that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Ion Battery M4605A and M4607A for use with IntelliVue Recalled by...
The Issue: The risk of battery failure increases with age, when a battery remains in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Frontier Natural Products Co-op Recalled by Frontier Natural Products...
The Issue: Testing of organic whole black peppercorns revealed the presence of Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: It has been identified that in a reject image workflow where multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy...
The Issue: Additional warning in the AMIA APD System labeling for patients vulnerable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iLab Ultrasound Imaging System Recalled by Boston Scientific Corporation Due...
The Issue: Specific iLab Ultrasound Imaging Systems using newest 3.0 (Polaris 1.0)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Imaging XS Syngo Imaging XS is a Picture Archiving Recalled by Siemens...
The Issue: A complaint reported that the archiving method at one customer site was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Digital Radiography X-Ray System Recalled by Shimadzu Medical...
The Issue: Shimadzu Corporation is recalling the Shimadzu Digital X-Ray System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Dynamics v9.5 system. A Picture Archiving and Communication System...
The Issue: Systems with the affected serial number are experiencing a software error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medrad Continuum MR Infusion system- non-wireless system The MEDRAD...
The Issue: There is a potential safety risk associated with potentially damaged locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Recalled by B....
The Issue: B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor with system software version...
The Issue: Software communication failure may occur on the HeartStart XL+ locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ACUSON X700 Ultrasound Systems with software version 1.0.00 Recalled...
The Issue: When fourSight 4D ultrasound imaging, 3-Scrape real time 3D imaging, or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...
The Issue: 1. ABACUS v3.1 may calculate quantities of electrolytes that are double the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Circular Lock Screws Recalled by Genesys Orthopedics Systems, LLC Due to The...
The Issue: The recall is being initiated because MK Precision (the Circular Lock Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.