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. 1,955 recalls have been distributed to Indiana in the last 12 months.
Showing 22821–22840 of 29,228 recalls
Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...
The Issue: Reports where patients who recently switched from the current Shiley...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0210-312-000-Woundcare Replacement kit with soft tip Recalled by Stryker...
The Issue: Potential sterility breach in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglycerides GPO. In vitro test for the quantitative determination of...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDL-Cholesterol gen.3. For the quantitative determination of high-density...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Plus ver. 2. Intended for use on COBAS INTEGRA systems Recalled...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDL-Cholesterol plus gen.3. Recalled by Roche Diagnostics Operations, Inc....
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LDL-Cholesterol gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uric Acid plus ver.2 In vitro test for the quantitative Recalled by Roche...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglycerides/Glycerol Blanked. In vitro test for the quantitative...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXPRESS Dry Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol Gen.2. The cassette COBAS Integra Cholesterol Gen.2 (CHOL2)...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate. Intended for use on COBAS INTEGRA 800 and 400 plus systems Recalled...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D2-40 (Lymphatic Marker) Recalled by Biocare Medical, LLC Due to Firm...
The Issue: Firm discovered that incorrect Instructions for Use were shipped with one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.