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. 2,455 recalls have been distributed to Indiana in the last 12 months.
Showing 46201–46220 of 53,528 recalls
Recalled Item: Puritan Bennett 840 ventilator systems software part number 4-070212-85...
The Issue: Covidien is conducting a voluntary field corrective action on Puritan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pyridostigmine Bromide Tablets USP Recalled by Corepharma LLC Due to Failed...
The Issue: Failed Dissolution Specification: Corepharma Inc. is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...
The Issue: Ensuring all customers have the tools to assist in verifying the setting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectible Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Glass defect located on the interior neck of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candy Sweet Spots Recalled by Bee International, Inc. Due to Undeclared Egg
The Issue: Bee International is recalling Sweet Spots Candy because it has undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: Sterility of medical devices intended for use in surgical procedures may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is Recalled...
The Issue: On December 13, 2012, King Systems initiated a voluntary recall of one (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrOXYzine HCI Tablets USP 10 mg Recalled by KVK-Tech, Inc. Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrOXYzine HCI Tablets USP 25 mg Recalled by KVK-Tech, Inc. Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrOXYzine HCI Tablets USP 50 mg Recalled by KVK-Tech, Inc. Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TSX-301C Aquilion One (Vision Edition) Computed Tomography X-Ray System....
The Issue: Toshiba America Medical Systems, Inc. initiated this recall due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx Gram-Negative QuickFISH BC. In-Vitro Diagnostic for the...
The Issue: Kits incompatible with certain fluorescence microscope light sources
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.