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. 2,134 recalls have been distributed to Indiana in the last 12 months.
Showing 7021–7040 of 53,528 recalls
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.2.100 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.3.000 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.2.200 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.1.000US Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.2.000 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Remedy Clinical TREAT Antifungal Cream Recalled by MEDLINE...
The Issue: Labeling: Not Elsewhere Classified; Product labeling contains the claim of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Protocol for Life Balance Recalled by Now Foods Due to Amount of...
The Issue: Amount of Phosphatidyl Serine in product is less than stated on the label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fosaprepitant for Injection 150 mg per vial Recalled by BE PHARMACEUTICALS...
The Issue: Lack of Sterility Assurance: Aseptic process simulation failure.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP.TROCAR W. DILATING PIN 10/110MM Recalled by Aesculap Inc Due to The...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP.HASSON TROCAR 12/110MM Recalled by Aesculap Inc Due to The sterile...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.