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. 1,739 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,739 in last 12 months

Showing 4870148720 of 51,038 recalls

Medical DeviceNovember 16, 2012· Praxair Inc.

Recalled Item: Praxair Vantage Grab n Go - Gas Cylinder pressure regulator Recalled by...

The Issue: Isolated incidents of ignition inside Grab n' Go cylinders that had been...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 16, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek 11 MM Fully Fluted Reamer Recalled by DePuy Mitek, Inc., a...

The Issue: Specific units of the DePuy Mitek Sterile Reamers are not labeled correctly,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· EEG Info

Recalled Item: EEG NeuroAmp Recalled by EEG Info Due to Mislabeling

The Issue: EEG Info, Inc. is recalling the EEG Neuroamp device because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Biomet, Inc.

Recalled Item: Biomet Offset Tibial Tray 2.5 mm Adaptor Recalled by Biomet, Inc. Due to...

The Issue: Biomet investigation identified that the square end of the offset tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V500 Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V100 Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V100-BGM Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· GE Healthcare It

Recalled Item: GE Centricity PACS Workstation Recalled by GE Healthcare It Due to While...

The Issue: While merging exams in a test instance, merges carry forward in the...

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

Class II — Potential Health HazardOngoing
DrugNovember 15, 2012· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible particulate and particulate embedded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur DHEA-504 (DHEAS) 50 Test 06489701 The...

The Issue: Operating range of the ADVIA Centaur systems is 18C to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: This notice is being provided in follow up to the field correction initiated...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2012· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas b 123 POC system cobas b 123 POC system Recalled by Roche Diagnostics...

The Issue: It has been determined that cobas b 123 Fluid Pack COOX cuvettes for lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur Folate (FOL) 500 Test 06891541 100 Recalled...

The Issue: Operating range of the ADVIA Centaur systems is 18C¿ to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare BR Assay for CA 27.29 250 Test Kits Recalled by Siemens...

The Issue: Operating range of the ADVIA Centaur systems is 18¿C to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing