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. 2,535 recalls have been distributed to Indiana in the last 12 months.
Showing 31801–31820 of 53,528 recalls
Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Agar (TSA w/ 5% Sheep Blood) Plate Recalled by Remel Inc Due to...
The Issue: Confirmed complaint of surface contamination of Listeria monocytogenes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i...
The Issue: It was discovered during a procedure that when the operator made an exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension Recalled by...
The Issue: Elevating Monitor Suspension column dropping and will not rise back up.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...
The Issue: Reported customer complaints of automated hematology analyzers catching fire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 mL Medallion¿ Syringe. Catalog Numbers: 701989001 Recalled by Merit...
The Issue: Merit Medical Systems announces a voluntary field action for the 1mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4% Recalled by...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pilocarpine Hydrochloride Ophthalmic Solution 4% Recalled by Novartis...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Aerosol Recalled by...
The Issue: Defective Delivery System: Elevated number of units with out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIA-360 Analyzer is capable of performing two methods of immunoassay:...
The Issue: The firm has become aware of a potential issue with the AIA-360 analyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.