Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,503 in last 12 months

Showing 1492114940 of 27,462 recalls

Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 (US)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.

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

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.

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

Recalled Item: CAPNOSTREAM 20P (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: 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 (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.

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: 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: 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.

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· Endologix

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.

Class I — Serious 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 20 (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: 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: 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.

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

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Endologix

Recalled Item: ENDOLOGIX AFX2 Bifurcated Endograft System Recalled by Endologix Due to...

The Issue: Endologix is notifying physicians of patient tailored surveillance...

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

Class I — Serious 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: 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: Capnostream20 (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.

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

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.

Class II — Potential Health HazardOngoing