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. 1,097 recalls have been distributed to Indiana in the last 12 months.
Showing 16061–16080 of 53,528 recalls
Recalled Item: Levetiracetam Tablets USP Recalled by McKesson Corporation dba McKesson Drug...
The Issue: Labeling; Wrong Barcode; error in the machine-readable barcode which could...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Edwards TruWave (30 cc)/VAMP Jr/52 in (132 cm) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (30 cc)/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards VAMP Jr. 6 in (15 cm) Recalled by Edwards Lifesciences, LLC Due to...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Physician Order Form (PL-15400-00 Recalled by Flowonix Medical Inc Due to...
The Issue: Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave 3 cc/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC Due...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Recalled by Edwards Lifesciences, LLC Due to There is a potential...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (3 cc)/VAMP Jr Recalled by Edwards Lifesciences, LLC Due to...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...
The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...
The Issue: Potential for mold contamination (Aspergillus vadensis)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giant Eagle Chicken Street Taco Kit Recalled by Giant Eagle, Inc. Due to...
The Issue: Undeclared egg allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ***Chicken Street Taco Kit with Trays Recalled by Reser's Fine Foods, Inc....
The Issue: Undeclared egg. The cup of Chipotle Crema in the Chicken Street Taco kits...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SUNSTAR G.U.M PERIOSHIELD Oral Health Rinse Recalled by Sunstar Americas,...
The Issue: Products may be contaminated with micro-organisms Burkholderia cepacia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Vantage Tiitan 1.5T with Standard gradient Recalled by Canon Medical...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Titan 3T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.