Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,466 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,466 in last 12 months

Showing 2474124760 of 49,677 recalls

Medical DeviceAugust 1, 2018· COVIDIEN LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2018· COVIDIEN LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2018· COVIDIEN LLC

Recalled Item: Kerlix Gauze 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2018· COVIDIEN LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2018· EOS Imaging

Recalled Item: sterEOS workstation Recalled by EOS Imaging Due to 3D projections may be...

The Issue: 3D projections may be incorrect when the pair of images used is a secondary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 M NICU (CPM) 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: CAPNOSTREAM 20P (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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: CAPNOSTREAM 20P (US) 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: CAPNOSTREAM 20P (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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 (INTL) M 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: CAPNOSTREAM 20P (US) 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 (US) M W/PRINTER TO MASIMO 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: CAPNOSTREAM 20P (US) 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 N CYVITAL 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 N 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 M ADULT ICU (CPM) 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.

Class II — Potential Health HazardOngoing