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 2348123500 of 28,245 recalls

Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: A trocar is a sharp-pointed instrument used with a cannula Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Tonometers are manual devices intended to measure intraocular pressure by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Cushing burrs are bone cutting and drilling instruments that are Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Manual trephines are bone cutting and drilling instruments that are Recalled...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Hudson cerebellar extensions are bone cutting and drilling instruments that...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Traction tong replacement screws Recalled by Instrumed International, Inc....

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Replacement screw non-springloaded traction tongs are skull tongs for...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Hudson braces are bone cutting and drilling instruments that are Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Lock nuts for titanium traction tongs are used in traction Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics (OCD) identified an anomaly with Software Version...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Ortho Clinical Diagnostics (OCD) identified an anomaly with Software Version...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Teleflex Medical

Recalled Item: Hudson RCI¿ Pediatric Anesthesia Breathing Circuits Recalled by Teleflex...

The Issue: The pediatric breathing circuits can crack prior to and during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has become aware of a potential safety issue involving missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2014· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: The software issue described was corrected in the modification to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2014· Midmark Corp dba Progeny Inc

Recalled Item: Vantage Panoramic X-Ray System used to perform dental and orthodontic...

The Issue: Failure of the primary collimator may result in unintentional movement of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2014· Teleflex Medical

Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...

The Issue: Misbranding: Although the product labeling identifies the catheters as...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF Recalled by...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing