Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,641 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,641 in last 12 months

Showing 4438144400 of 47,027 recalls

FoodFebruary 4, 2013· Aptalis Pharma Us Inc

Recalled Item: SourceCF(R) Pediatric Drops Recalled by Aptalis Pharma Us Inc Due to The...

The Issue: The data suggests that the formulation does not support the shelf life of...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2013· American Health Packaging

Recalled Item: buPROPion Hydrochloride Extended Release Tablets Recalled by American Health...

The Issue: Failed Stability Specifications; out of specification results at the 9 month...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 4, 2013· Carib Import & Export, Inc.

Recalled Item: Benjamins Infants Gripe Mixture Recalled by Carib Import & Export, Inc. Due...

The Issue: CGMP Deviations: this product is being recalled because an FDA inspection...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2013· Endogastric Solutions Inc

Recalled Item: EndoGastric Solutions EsophyX2 Plus Device with Serosa Fastener and...

The Issue: EsophyX2Plus device was not validated under actual or simulated use...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Hyperbaric Infusion System is a cassette based Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and...

The Issue: The firm has received numerous complaints of the cannulated screw driver tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing