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. 2,752 recalls have been distributed to Indiana in the last 12 months.
Showing 3561–3580 of 29,228 recalls
Recalled Item: Aisys CS2. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2 with Et Control. This anesthesia gas machine is Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 100. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavaClick Syringe and Needle Recalled by LINEAGE BIOMEDICAL, INC Due to...
The Issue: Incorrect GTIN number on carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avance CS2 and Avance CS2 Pro. These anesthesia gas machines Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys. This anesthesia gas machine is intended to provide general Recalled...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avance. This anesthesia gas machine is intended to provide general Recalled...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amingo. OUS only. Recalled by Datex-Ohmeda, Inc. Due to Potential issue that...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 7900. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire View. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...
The Issue: Due to mislabeling of products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...
The Issue: Due to mislabeling of products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VITROS XT Chemistry Products ALB-TP Slides is a single Recalled by...
The Issue: The reason for this recall is QuidelOrtho has determined that during normal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidewire 70cm x 1mm (0.038 ) These accessories Recalled by Bard Peripheral...
The Issue: Due to guidewires being manufactured incorrectly with the guidewires being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...
The Issue: Due to a software issues, after the instrument processes 250 racks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Recalled by Integra LifeSciences Corp. Due to Specific...
The Issue: Specific lots of TruDi NAV Suction Instruments 0 Degrees were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora 4 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.