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. 2,547 recalls have been distributed to Indiana in the last 12 months.
Showing 27141–27160 of 53,528 recalls
Recalled Item: Endo GIA 45mm Curved Tip Articulating Vascular/Medium Reload with Tri-Staple...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Assayed Specific Protein Control - Level 2 (SP Control 2)...
The Issue: The recalling firm has confirmed that Free Kappa light chains in Liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Assayed Specific Protein Control - Level 1 (SP Control 1)...
The Issue: The recalling firm has confirmed that Free Kappa light chains in Liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Assayed Specific Protein Control - Level 3 (SP Control 3)...
The Issue: The recalling firm has confirmed that Free Kappa light chains in Liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer Dark Chocolate Covered Almonds Recalled by Meijer, Inc #816 - Grand...
The Issue: Meijer initiated a voluntary recall of Dark Chocolate Covered Almonds due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...
The Issue: The block used to connect the patient pallet to the couch may be assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...
The Issue: Potential for control line not appearing on the test strip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...
The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...
The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Modular Primary Tibial Tray Implants Recalled by Zimmer Biomet, Inc....
The Issue: One lot of 75mm tibial tray is potentially etched and labeled as a 79 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7K capsules packaged in single packs sold in 24-count boxes Recalled by...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.