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. 2,507 recalls have been distributed to Indiana in the last 12 months.
Showing 35981–36000 of 53,528 recalls
Recalled Item: Fentanyl Citrate 2mcg/mL & 0.2% Ropivacaine HCI in 0.9% Sodium Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupivacaine 1mg/mL injection in 0.9% Sodium Chloride 250 mL bag Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate injection Recalled by Pharmakon Pharmaceuticals, Inc. Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine HCI 0.2% in 0.9% Sodium Chloride Recalled by Pharmakon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCL 1.25 GM added to 5% Dextrose in a 250 mL lntravia bag...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acorn 130 Stairlift Recalled by Acorn Stairlifts, Inc Due to The design of...
The Issue: The design of the seats did not consistently have the adequate strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging...
The Issue: Dietary Supplements contain undeclared milk and soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Life's Qik Fix 70 Plant Minerals Plus 80 Additional Nutrients Recalled by...
The Issue: Dietary Supplements contain undeclared milk and soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nuvi Global StemVitae Multivitamin 30oz. Recalled by Nuvi Global Corporation...
The Issue: Undeclared whey protein which contains the allergens of milk and soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The VITROS¿ Chemistry Products Calibrator Kit 31 Recalled by Ortho-Clinical...
The Issue: There is an incorrect value (data/calibration mathematics) on ADDs. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional Recalled...
The Issue: The Surgical Table Cushion (HybriGel Pads) could potentially contain staples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radionuclide Radiation Therapy System Product The product is a teletherapy...
The Issue: The latches of the frame adapter can be locked even if the locating pins of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm Three-fluted drill bit Recalled by Synthes (USA) Products LLC Due to...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...
The Issue: Defective Container: Excess lidding material accumulation between the seal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Transluminal Biliary Biopsy Forceps Set Forceps Recalled by Cook Inc. Due to...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White Lumax Guiding Coaxial Catheter Catheter Recalled by Cook Inc. Due to...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software. The firm name on the label is Recalled by Merge...
The Issue: There are potential issues with results reporting for certain run-based...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00720504022 ACETAB.CUPW/SH Recalled by Zimmer Trabecular Metal Technology,...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.