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. 2,322 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,322 in last 12 months

Showing 3166131680 of 47,027 recalls

Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA GDE/UIM upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: Gas Delivery Engine (GDE)-1st Generation Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard ventilator- Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Comprehensive ventilator- Recalled by Carefusion 211 Inc dba Carefusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Zimmer Gmbh

Recalled Item: Dome Centric component ( 01.04227.005) from the Anatomical Shoulder (AS)...

The Issue: In some cases it has been difficult or not possible to disassemble the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA GDE upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due to...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Comprehensive ventilator Recalled by Carefusion 211 Inc dba Carefusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard with Compressor ventilator Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Akorn, Inc.

Recalled Item: Sulfacetamide Sodium Ophthalmic Solution Recalled by Akorn, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility; some lots failed Antimicrobial Effectiveness...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 16, 2016· Virtus Pharmaceuticals, Llc

Recalled Item: VP-CH-PNV Prenatal/Postnatal capsules Recalled by Virtus Pharmaceuticals,...

The Issue: Defective delivery system: Softgel capsules are leaking.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 16, 2016· FSC Laboratories, Inc

Recalled Item: Flexichamber Anti-Static Valved Collapsible Holding Chamber Recalled by FSC...

The Issue: Product had torn/loose seal around the mouthpiece.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics...

The Issue: If the user selects the Comment or Interpretation option (in the enGEN .gsb...

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

Class III — Low RiskOngoing
FoodMay 13, 2016· Dr. Praeger'S Sensible Foods

Recalled Item: Dr. Praeger's California Veggie Burgers Recalled by Dr. Praeger'S Sensible...

The Issue: Dr. Praeger's Sensible Food/Ungar's Food Products is voluntarily recalling...

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

Class I — Serious Health HazardOngoing
Refund