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. 1,916 recalls have been distributed to Indiana in the last 12 months.
Showing 27201–27220 of 29,228 recalls
Recalled Item: A) Product Code 2N1191: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Obturator Product...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro/ Sure-Pro Ultra Embryo Replacement Catheters (with...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Single Stage Embryo Replacement Catheter Product Code:...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner and Reprocessor System Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter with Obturator...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N8371: Non-DEHP Y-Type Catheter Extension Set Kit Recalled...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Stylet Product...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Corp. AxSOS System Instrument. The AxSOS Locking...
The Issue: Stryker Orthopaedics has received a report indicating that the scale of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCS3011 AV Loop Kit For use with Transonic CO status System Only Recalled by...
The Issue: Transonic Systems Inc. have received complaints of blood leakage involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...
The Issue: The problem is that the "static tolerances" from the calibration files...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...
The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Irrigator Reusable Tips: Vented Tip Recalled by Stryker Endoscopy...
The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Irrigator Reusable Tips: 2mm X 34cm Regular Tip with No Hole...
The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 32cm Hydrodissection Tip Recalled by...
The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 24cm Regular Tip Recalled by Stryker...
The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Irrigator Reusable Tips: 10mm X 32cm Pool Suction Tip Recalled by...
The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.