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. 2,445 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,445 in last 12 months

Showing 2438124400 of 28,245 recalls

Medical DeviceApril 9, 2014· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae Recalled by...

The Issue: Potential for separation of dilator tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When the E-NMT-01 module...

The Issue: When the E-NMT-01 module is used in conjunction with the ElectroSensor, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Cochlear Americas Inc.

Recalled Item: Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to Recalled by...

The Issue: Cochlear America is recalling Cochlear Baha Soft Tissue Gauge due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo...

The Issue: Potential for separation of dilator tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Bio-Rad Laboratories, Inc.

Recalled Item: Variant II beta-thalassemia Short Program Model Numbers 270-2103 (250 tests)...

The Issue: There is an issue with the buffers which impacts the quantification of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Philips Medical Systems, Inc.

Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...

The Issue: In special cases, during the start-up of the current model of MobileDiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam -emission computed tomography system Used to detect or image Recalled...

The Issue: There is a potential for patient finger injury on the e.cam systems.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 Recalled...

The Issue: Siemens investigation confirmed that a portion one lot of panel Pos Combo 33...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2014· Small Bone Innovations, Inc.

Recalled Item: SBi RingFix Olive Wires Product Usage: These are temporary devices Recalled...

The Issue: Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2014· Western / Scott Fetzer Company

Recalled Item: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)...

The Issue: Separation events have occurred, including the VIPR separating from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2014· Abbott Laboratories, Inc

Recalled Item: Lipase Reagent Recalled by Abbott Laboratories, Inc Due to Package inserts...

The Issue: Package inserts have incorrect SmartWash parameters for Triglyceride.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2014· Medtronic Neuromodulation

Recalled Item: Kit 8551/856X (includes Models 8561 Recalled by Medtronic Neuromodulation...

The Issue: Some kits in the affected lots may contain an extension tubing set that is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2014· Philips Medical Systems, Inc.

Recalled Item: Lithium Ion Battery M4605A and M4607A for use with IntelliVue Recalled by...

The Issue: The risk of battery failure increases with age, when a battery remains in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Dynamics v9.5 system. A Picture Archiving and Communication System...

The Issue: Systems with the affected serial number are experiencing a software error...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Imaging XS Syngo Imaging XS is a Picture Archiving Recalled by Siemens...

The Issue: A complaint reported that the archiving method at one customer site was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2014· Bayer Corp

Recalled Item: Medrad Continuum MR Infusion system- non-wireless system The MEDRAD...

The Issue: There is a potential safety risk associated with potentially damaged locking...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2014· Baxter Healthcare Corp.

Recalled Item: AMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy...

The Issue: Additional warning in the AMIA APD System labeling for patients vulnerable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2014· GE Healthcare

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: It has been identified that in a reject image workflow where multiple...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2014· B. Braun Medical, Inc.

Recalled Item: Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Recalled by B....

The Issue: B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2014· Shimadzu Medical Systems

Recalled Item: Shimadzu Digital Radiography X-Ray System Recalled by Shimadzu Medical...

The Issue: Shimadzu Corporation is recalling the Shimadzu Digital X-Ray System because...

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

Class II — Potential Health HazardOngoing