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. 1,129 recalls have been distributed to Indiana in the last 12 months.
Showing 8141–8160 of 29,228 recalls
Recalled Item: 3M SYSTAGENIX/KCI KerraCel Ag DRESSING Recalled by Mckesson Medical-Surgical...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Monofilament Manufacturing MONOFILIMENT TEST Recalled by Mckesson...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Comply INDICATOR Recalled by Mckesson Medical-Surgical Inc. Corporate...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical PREFILTER Recalled by Mckesson Medical-Surgical Inc....
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Skin Adhesive McKesson LiquiBand Exceed 0.4 mL Liquid Dome Recalled by...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. SPS MEDICAL SUPPLY Steam Indicator Strip SPSmedical Sterilization...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING Recalled by Mckesson...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with...
The Issue: The automated dispensing cabinet software update included a .dll file that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: t:slim X2 insulin pump Recalled by Tandem Diabetes Care Inc Due to Insulin...
The Issue: Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283)...
The Issue: It may occur that after system startup no stand movement is possible any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02) Recalled...
The Issue: There is a risk that blind screws of the modular tibial component cannot be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: t:slim X2 insulin pump Recalled by Tandem Diabetes Care Inc Due to Insulin...
The Issue: Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Model Modular Femur and Tibia Recalled by Waldemar Link GmbH & Co. KG...
The Issue: There is a risk that blind screws of the modular tibial component cannot be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Modular. orthopedic prosthesis. Model Nos: Small Recalled...
The Issue: There is a risk that blind screws of the modular tibial component cannot be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component. orthopedic prosthesis. Model Nos: Small Recalled by...
The Issue: There is a risk that blind screws of the modular tibial component cannot be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 770G Insulin Pump (U.S. and O.U.S. Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 720G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 780G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.