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 2664126660 of 51,038 recalls

Medical DeviceMay 16, 2018· Elekta, Inc.

Recalled Item: HexaPOD evo RT Couch Top (also known as HexaPOD evo Module) Recalled by...

The Issue: Upon completion of a 6D workflow, the HexaPOD evo Module may be in a tilted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BEAD TIP GD WIRE 3.0MM X 60CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: RECON DRILL 6MM X 439MM Recalled by Zimmer Biomet, Inc. Due to The firm is...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BALL TIP GUIDE WIRE 3.2MMX55CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: G-PIN 2.8BL 3.2PL 60CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: G-PIN 2.8BL 3.2PL 98CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BALL TIP GUIDE WIRE 3.2MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2018· CAREstream Medical LLC

Recalled Item: CAREstream ProNox Nitrous Oxide Delivery System labeled as the following:...

The Issue: Two analgesic gas delivery system oxygen/nitrous oxide mixers were reported...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2018· Draeger Medical Systems, Inc.

Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...

The Issue: Users have misinterpreted the display for out of range measurement indicated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 15, 2018· Draeger Medical Systems, Inc.

Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...

The Issue: Users have misinterpreted the display for out of range measurement indicated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 15, 2018· Megadyne Medical Products, Inc.

Recalled Item: MegaPower Electrosurgical Generator Recalled by Megadyne Medical Products,...

The Issue: If two devices are plugged into the same channel/port in the generator, both...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2018· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: XLTEK EMU40EX EEG Headbox Recalled by Natus Neurology DBA Excel Tech., Ltd....

The Issue: Possible degradation of an internal electronic component over time which may...

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

Class II — Potential Health HazardOngoing
DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Teething Drops Recalled by MBi Distributing Inc. dba MBi Nutraceuticals Due...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Argentum Elixir Colloidal Silver Recalled by MBi Distributing Inc. dba MBi...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Expectorant Cough Syrup Recalled by MBi Distributing Inc. dba MBi...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Silver-Zinc Throat Spray Recalled by MBi Distributing Inc. dba MBi...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Nausea Drops Recalled by MBi Distributing Inc. dba MBi Nutraceuticals Due to...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Stomach Calm Recalled by MBi Distributing Inc. dba MBi Nutraceuticals Due to...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Intestinal Colic Drops Recalled by MBi Distributing Inc. dba MBi...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 14, 2018· Merck Millipore Ltd.

Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...

The Issue: In vitro diagnostic devices, used greater than 6 months after date of...

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

Class II — Potential Health HazardOngoing