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. 960 recalls have been distributed to Indiana in the last 12 months.
Showing 47861–47880 of 53,528 recalls
Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...
The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...
The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Luer Lock Cap The device is intended for use Recalled by Baxter...
The Issue: The firm is recalling lots 10043 and 10044 due to loose particulate matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...
The Issue: Expired active ingredient was used in the manufacture of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...
The Issue: STERIS has identified that the population of the G. stearothermophilus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...
The Issue: Integra LifeSciences has identified through an internal evaluation that in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...
The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talenti German Chocolate Cake Gelato Recalled by Talenti Gelato Due to...
The Issue: Product contains undeclared Allergen; Almonds.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi for Her 50+ (Full Strength Mini and Multi softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi For Him (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi Complete (Full Strength Mini and Multi Softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube Recalled by Becton...
The Issue: An in-vitro diagnostic reagent may be labeled with an incorrect barcode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.