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. 2,697 recalls have been distributed to Indiana in the last 12 months.
Showing 11961–11980 of 53,528 recalls
Recalled Item: Difluprednate Ophthalmic Emulsion Recalled by CIPLA Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: customer complaint for defective container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Dr....
The Issue: FAILED DISSOLUTION SPECIFICATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Pfizer Inc. Due to Presence of...
The Issue: Presence of particulate matter: particulate identified as a beetle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Dr....
The Issue: FAILED DISSOLUTION SPECIFICATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ProPlan CMF Anatomical Model Recalled by Materialise USA LLC Due to...
The Issue: MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grappler Suture Anchor Recalled by Paragon 28, Inc. Due to Suture anchor may...
The Issue: Suture anchor may break upon insertion, which could lead to potential debris...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kingdom Honey Royal Honey VIP The Ultimate Power Source Recalled by...
The Issue: Undeclared Sildenafil
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Woodland Ingredients X06D Arborio Rice Recalled by Woodland Foods LLC Due to...
The Issue: possible presence of glass pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surpria 64: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...
The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surpria: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tacrolimus Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Defective Container: Tube split from side seam
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ativan Injection (lorazepam injection Recalled by Hikma Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.