Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,054 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,054 in last 12 months

Showing 15241–15260 of 28,245 recalls

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: 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: Capnostream20 (US) M TO MASIMO 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 (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 (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 (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 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 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 (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.

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

Recalled Item: Capnostream20 (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 30, 2018· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Complaints received of sporadic erroneously elevated platelet results...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2018· Zimmer Biomet Spine Inc.

Recalled Item: Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system...

The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2018· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Complaints received of sporadic erroneously elevated platelet results...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2018· Zimmer Biomet Spine Inc.

Recalled Item: Vitality¿ Spinal Fixation System. Spinal Interlaminal Recalled by Zimmer...

The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2018· Beckman Coulter Inc.

Recalled Item: UniCel DxH 900 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Complaints received of sporadic erroneously elevated platelet results...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2018· Zimmer Biomet Spine Inc.

Recalled Item: Vitality¿ Spinal Fixation System.Spinal Intervertebral Body Recalled by...

The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Interventional Fluoroscopic X-Ray System Recalled by Siemens Medical...

The Issue: Temperature of the detector may fall out of its designed working range (cool...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno Interventional Fluoroscopic X-Ray System Recalled by Siemens...

The Issue: Temperature of the detector may fall out of its designed working range (cool...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2018· Sysmex America, Inc.

Recalled Item: Sysmex XN-Series Fluorocell PLT Recalled by Sysmex America, Inc. Due to The...

The Issue: The fluorescent platelet counts (PLT-F) and immature platelet fraction (IPF)...

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

Class II — Potential Health HazardOngoing