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. 1,978 recalls have been distributed to Indiana in the last 12 months.
Showing 17561–17580 of 29,228 recalls
Recalled Item: Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿¿ ¿¿¿ ¿¿¿...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Prefilled 550 ml Sterile¿¿ ¿ Recalled by Medex Cardio-Pulmonary...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 1000 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Unit Dose 5 ml Normal Saline (0.9%)¿¿¿¿ ¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intermed 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ ¿¿¿ Recalled...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline 300-350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿ Recalled by...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Unit Dose 15 ml Normal Saline ¿ Recalled by Medex Cardio-Pulmonary...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ Recalled by...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink Series EF+ Oral Sleep Apnea Device. Recalled by Respire Medical...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink+ Hard/Soft Oral Sleep Apnea Device Recalled by Respire Medical...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink H/S Oral Sleep Apnea Device Recalled by Respire Medical Due to...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ELAN 4 Air System is intended for high speed cutting Recalled by...
The Issue: The ELAN 4 Air System was released to the market place prior to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink+ Hard Oral Sleep Apnea Device Recalled by Respire Medical Due...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink H/S Oral Sleep Apnea Device Recalled by Respire Medical Due to...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated Peritoneal Dialysis Set with Cassette Recalled by...
The Issue: The firm received increased customer complaints for Missing Red Line,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500 Recalled by...
The Issue: There is a potential failure of the top plate assembly, which is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.