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. 2,577 recalls have been distributed to Indiana in the last 12 months.
Showing 21061–21080 of 53,528 recalls
Recalled Item: HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube - Product Recalled by...
The Issue: The tracheal and brochial swivel connectors are incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive...
The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroDot brand: Wave Prep Single use cups Recalled by Bio-Signal Group Corp....
The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of...
The Issue: Current software version of the Anti-HAV IgM APP-file (version 06.05-101)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer Private Label Item Code: 3069 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code: 303063 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lannett Ranitidine Syrup (Ranitidine Oral Solution Recalled by Lannett...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE INJECTION Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 500 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 100 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 14MM- Orthopedic...
The Issue: Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 -...
The Issue: Medial and lateral polyethylene inserts did not securely fit into the cobalt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The...
The Issue: During the firm's review of May 2019 complaint data, a significant increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic...
The Issue: Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.