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. 936 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
936 in last 12 months

Showing 48521–48540 of 51,038 recalls

FoodDecember 21, 2012· NBTY Inc.

Recalled Item: MET-Rx EXTREME THERMO RAGE WATERMELON DIETARY SUPPLEMENT Recalled by NBTY...

The Issue: Acetobacter lovaniensis was detected in a sample of the product tested by a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodDecember 21, 2012· Dollar Tree Distribution, Inc.

Recalled Item: Candy Canes Recalled by Dollar Tree Distribution, Inc. Due to Candy product...

The Issue: Candy product may contain metal and/or plastic pieces embedded in the candy.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2012· Dollar Tree Distribution, Inc.

Recalled Item: Candy Canes Recalled by Dollar Tree Distribution, Inc. Due to Candy product...

The Issue: Candy product may contain metal and/or plastic pieces embedded in the candy.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2012· NBTY Inc.

Recalled Item: PURE PROTEIN PROTEIN SHOT 25g PROTEIN Recalled by NBTY Inc. Due to...

The Issue: Lactobacillus plantarum and Lactobacillus brevis were detected in a sample...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 20, 2012· Medisystems a NX Stage Company

Recalled Item: Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Recalled by...

The Issue: A total of 5 (ea) single needle pouches are mislabeled as 15 Ga x1" instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Medisystems a NX Stage Company

Recalled Item: Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Recalled by...

The Issue: Single needle packs in each case ( 10 needles per case) are mislabeled on...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Philips Healthcare received reports from the field stating the patient table...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Concentric Medical Inc

Recalled Item: FlowGate Balloon Guide Catheter Recalled by Concentric Medical Inc Due to...

The Issue: Firm received complaints of resistance and possible collapse of the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Total Iron Binding Capacity (IBCT) Flex Reagent Cartridge. An...

The Issue: The analytical sensitivity claim of 6 ug/dL (1.1 umol/L) in the Instructions...

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

Class III — Low RiskOngoing
Medical DeviceDecember 20, 2012· Abbott Medical Optics Inc (AMO)

Recalled Item: AMO Sensar Intraocular Lenses (IOLs) Recalled by Abbott Medical Optics Inc...

The Issue: Two production orders of these IOLs that contain mislabeled IOLs.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Carefusion 303 Inc

Recalled Item: CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer...

The Issue: CareFusion is recalling the SmartSite¿ Gravity Blood Set as a result of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Healthtronics, Inc.

Recalled Item: HealthTronics Endocare 3.8mm RenalCryo Cryoprobe Recalled by Healthtronics,...

The Issue: The Endocare 3.8mm RenalCryo Cryoprobe is being recalled because the label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog...

The Issue: Reports of handle fracture and subsequent disassociation of cam assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) IRON Calibrator (DC85) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has received complaints of IRON calibrations...

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

Class III — Low RiskOngoing
Medical DeviceDecember 19, 2012· Elekta, Inc.

Recalled Item: Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1...

The Issue: The DICOM tags do not contain sufficient information for XVI to identify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R)...

The Issue: Siemens has confirmed an increase on absorbance errors when calibrating...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Hamilton Medical Inc

Recalled Item: HAMILTON-T1 Ventilator with software versions 1.1.2 or lower. The HAMILTON...

The Issue: Analysis of a customer complaint has shown that during ventilation of small...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Abbott Laboratories, Inc

Recalled Item: ARCHITECT HBsAg Qualitative Assay Recalled by Abbott Laboratories, Inc Due...

The Issue: Abbott has identified that assay files for the ARCHITECT HBsAg Qualitative...

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

Class II — Potential Health HazardOngoing