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. 2,526 recalls have been distributed to Indiana in the last 12 months.
Showing 34341–34360 of 53,528 recalls
Recalled Item: Honeywell eyesaline Eyewash Sterile Isotonic Solution Recalled by Sperian...
The Issue: Non Sterility; contaminated with Klebsiella pneumoniae
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOBUTamine Injection Recalled by Hospira Inc. Due to Discoloration: Firm...
The Issue: Discoloration: Firm received complaints of product discoloration and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pentax Video Colonoscope is intended to be used with a Recalled by Pentax of...
The Issue: Pentax is initiating the product correction of several model numbers of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Gastroscope is intended to be used with a Recalled by Pentax of...
The Issue: PENTAX Medical is initiating this field action to provide customers that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific QMS Everolimus Assay Recalled by Microgenics Corporation...
The Issue: A reagent stability issue (still under investigation) causes less separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BruxZir Shaded Recalled by Prismatik Dentalcraft, Inc Due to Prismatik...
The Issue: Prismatik Dentalcraft is recalling BruxZir Shaded because the new design was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZATARAINS WHITE CHEDDAR CHIPOTLE PASTA DINNER 6 OZ PACKAGE Recalled by...
The Issue: The Zatarains plant in Gretna, LA was contacted by General Mills to inform...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ZATARAINS SOUTHERN STROGANOFF PASTA DINNER 6.5 OZ. PACKAGE Recalled by...
The Issue: The Zatarains plant in Gretna, LA was contacted by General Mills to inform...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ZATARAINS SCAMPI PASTA DINNER 5.2 OZ PACKAGE Recalled by McCormick & Company...
The Issue: The Zatarains plant in Gretna, LA was contacted by General Mills to inform...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ZATARAINS GUMBO PASTA DINNER 5.7 OZ PACKAGE Recalled by McCormick & Company...
The Issue: The Zatarains plant in Gretna, LA was contacted by General Mills to inform...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics, Inc. notified customers of erroneous results of VMA tests...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Fluid Management Set Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for Fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a...
The Issue: Post Market Surveillance cases reported to Maquet showing instances in which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCR Compano Basic Reader using 100-127V as mains voltage. Model numbers:...
The Issue: A defect component of the Compano reader power supply can cause the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS versions 8.4.7 Recalled by Novarad Corporation Due to Novarad...
The Issue: Novarad Corporation announces a voluntary field action for the NovaPACS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25 gauge VersaVit 2.0 Core Essentials Procedure Pack Recalled by Synergetics...
The Issue: Vitrectomy cutters have been found not to be operating within the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products TRIG Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25 gauge VersaVit 2.0 Procedure Pack with Photon Wide Field Illuminator...
The Issue: Vitrectomy cutters have been found not to be operating within the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.