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. 2,604 recalls have been distributed to Indiana in the last 12 months.
Showing 18421–18440 of 53,528 recalls
Recalled Item: Whole Foods Market Artequeso Manchego 6 month aged raw Raw Recalled by Whole...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market IL FORTETO Genovese Pesto PLU 20017100000 Individual...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market La Marquesa Herb Manchego Raw Milk - Recalled by Whole...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market AGRIFORM PIAVE VECCHIO PLU 29336200000 Individual sliced...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market El Trigal 12 Month Old Manchego PLU 29329500000 Recalled...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market Mitica Mahon PLU 29341800000 Individual sliced cheese...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC...
The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ Recalled by Open...
The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol) Recalled...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gluten-Free Organic Mesa Sunrise Cereal USA Recalled by Natures Path Foods...
The Issue: Undeclared Wheat and/or Barley.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab Cakes***48-3...
The Issue: Product contains undeclared hydrolyzed soy protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RSP Standard HUMERAL SOCKET INSERT Recalled by Encore Medical, LP Due to...
The Issue: Product may be mislabeled with the size etched onto products differing from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSP Standard HUMERAL SOCKET INSERT Recalled by Encore Medical, LP Due to...
The Issue: Product may be mislabeled with the size etched onto products differing from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience AIA-PACK BHCG Calibration Verification Test Set-In Vitro...
The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) Recalled by Maquet...
The Issue: Instruction For Use (IFU) incorrect serial number of 90437000. It should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...
The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...
The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.