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. 2,768 recalls have been distributed to Indiana in the last 12 months.
Showing 741–760 of 29,228 recalls
Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ LVAS Implant Kit Recalled...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound System 1300 Recalled by B-K Medical A/S Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk5000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UUltrasound System 2300 Recalled by B-K Medical A/S Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1202 Flex Focus Ultrasound System Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk3000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk3500 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: or BS737162 Automated Digital Cell Morphology analyzer DI-60 Recalled by...
The Issue: Automated cell-locating device barcode reader may read the barcode of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Lithotriptor Recalled by Olympus Corporation of the Americas Due...
The Issue: The device may either fail to start up, or the transducer may start briefly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SimplyGo Mini Recalled by Philips Respironics, Inc. Due to Certain serial...
The Issue: Certain serial numbers of the SimplyGo Mini standard battery kit contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM85 Digital Mobile X-ray imaging System Recalled by NeuroLogica Corporation...
The Issue: The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Good Neighbor Pharmacy Recalled by Trividia Health, Inc. Due to...
The Issue: Manufacturing defect causing LCD display issues with missing or partial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control...
The Issue: A labeling error was identified on the affected product. The expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Food Panel 3 Specific Allergen Recalled by Siemens Healthcare Diagnostics,...
The Issue: The barcode orientation on affected devices causes incorrect scanning order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...
The Issue: The nasal feeding tube may be occluded
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...
The Issue: The nasal feeding tube may be occluded
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...
The Issue: The nasal feeding tube may be occluded
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400...
The Issue: Sterility compromised from small holes that may occur during packaging of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...
The Issue: The nasal feeding tube may be occluded
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.