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 15461–15480 of 53,528 recalls
Recalled Item: REGARD Vitrectomy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook¿ Pump 15 Drop 0.2 Micron Filtered IV Set with Recalled by B. Braun...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Basic Cataract tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Core Biopsy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Ultrasound Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OUTLOOK PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Ear Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Pump Measured Volume Solution Set/ w/ Auto Shut-Off. Single-use...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OUTLOOK PUMP IV SET W/UNIVERSAL SPIKE-single-use for use with the Recalled...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT CUT GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET82HP OUTLOOK PUMP EXTENSION SET-single-use for use with the Outlook...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access hsTnI High Sensitivity Troponin I Recalled by Beckman Coulter Inc....
The Issue: Through customer feedback, testing a sample with cardiac troponin I...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.