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. 2,704 recalls have been distributed to Indiana in the last 12 months.
Showing 11321–11340 of 29,228 recalls
Recalled Item: Dual Mobility Vivacit-E Bearing Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The outer package is labeled as a Size C 38 mm, however, the implant inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...
The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture Recalled...
The Issue: Possible false negative or false positive results. The incorrect sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...
The Issue: Masks processed at one site were not maintained at levels of condensation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP Recalled...
The Issue: Due to non-surgical isolation gowns not meeting all performance test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra/Phonic Focus BP Conforming Gel Pads Recalled by Pharmaceutical...
The Issue: The firm registered the product as a Class I device, but has since been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...
The Issue: Connector between support surface and pump may be out of tolerance resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Dehydrognease P-L Recalled by Randox Laboratories Ltd. Due to An...
The Issue: An update to the carryover avoidance technical bulletin to introduce...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Dehydrogenase L-P Recalled by Randox Laboratories Ltd. Due to An...
The Issue: An update to the carryover avoidance technical bulletin to introduce...
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: 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.