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. 2,547 recalls have been distributed to Indiana in the last 12 months.
Showing 25781–25800 of 53,528 recalls
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module...
The Issue: A software malfunction of the infuser when used with a MedNet Custom Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix AMD Antimicrobial Bandage Roll Recalled by COVIDIEN LLC Due to...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (10 mL Size) Recalled by Instrumentation Laboratory Co....
The Issue: There is a potential for increased imprecision, out of range quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Air Optix Night & Day Aqua (lotrafilcon A) Recalled by Allied Vision...
The Issue: Potentially counterfeit products in/and counterfeit packaging were imported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (US) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 (US) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due to...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (INTL) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOLOGIX AFX/AFX2 Recalled by Endologix Due to Endologix is notifying...
The Issue: Endologix is notifying physicians of patient tailored surveillance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (COV-INTL) N W/PRINTER ROHS Recalled by Oridion Medical 1987...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20 (INTL) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (INTL) N - ROHS Recalled by Oridion Medical 1987 Ltd. Due to...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 (INTL) M Recalled by Oridion Medical 1987 Ltd. Due to The...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 (INTL) N Recalled by Oridion Medical 1987 Ltd. Due to The...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 M W/PRINTER CYVITAL Recalled by Oridion Medical 1987 Ltd. Due...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOLOGIX AFX/AFX2 Recalled by Endologix Due to Endologix is notifying...
The Issue: Endologix is notifying physicians of patient tailored surveillance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20 (INTL) N Recalled by Oridion Medical 1987 Ltd. Due to The...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (US) N - ROHS Recalled by Oridion Medical 1987 Ltd. Due to...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (INTL) N - ROHS Recalled by Oridion Medical 1987 Ltd. Due to...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.