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. 2,515 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,515 in last 12 months

Showing 53615380 of 47,027 recalls

Medical DeviceMay 15, 2024· Hamilton Medical AG

Recalled Item: Ventilator HAMILTON-C6 Recalled by Hamilton Medical AG Due to Ventilator may...

The Issue: Ventilator may enter sensor fail mode, ventilation may not re-initiate,...

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

Class I — Serious Health HazardOngoing
DrugMay 14, 2024· Imprimis NJOF, LLC

Recalled Item: Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic Suspension Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 14, 2024· Imprimis NJOF, LLC

Recalled Item: Moxifloxacin 4 mg/0.8 mL Preservative-Free 0.8mL Single-Use vials for...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 14, 2024· Imprimis NJOF, LLC

Recalled Item: Klarity-C (cyclosporine) Preservative-Free Sterile Ophthalmic Emulsion 0.1%...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 14, 2024· Imprimis NJOF, LLC

Recalled Item: Dexamethasone-Moxifloxacin- Ketorolac (1mg/mL Recalled by Imprimis NJOF, LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 14, 2024· Imprimis NJOF, LLC

Recalled Item: Moxifloxacin 0.8 mg/0.8 mL Preservative-Free 0.8mL Single-Use vials for...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 14, 2024· Imprimis NJOF, LLC

Recalled Item: Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free 1mL...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 14, 2024· Imprimis NJOF, LLC

Recalled Item: Dexamethasone-Moxifloxacin (1 mg/mL and 5mg/mL) Preservative-Free Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 14, 2024· Imprimis NJOF, LLC

Recalled Item: Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free 1mL...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 14, 2024· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 Recalled by...

The Issue: The firm received reports that some blood collection tubes have experienced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate...

The Issue: Kit assigned an extended expiration date of 24-Jul-2025 during release. The...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2024· Applied Medical Technology Inc

Recalled Item: AMT Initial Placement Dilator Set. Used to place gastrostomy devices....

The Issue: Devices were labelled with the incorrect guidewire labelling.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2024· NxStage Medical Inc

Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical Inc Due to The...

The Issue: The smaller chamber of the two chamber bag is bursting when nurses are...

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

Class II — Potential Health HazardOngoing
DrugMay 13, 2024· Golden State Medical Supply Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Golden State Medical Supply...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets Recalled by Glenmark...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets Recalled by Glenmark...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2024· American Regent, Inc.

Recalled Item: Vasopressin Injection Recalled by American Regent, Inc. Due to Subpotent...

The Issue: Subpotent product in addition to having out-of-specification results for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 13, 2024· SVS LLC

Recalled Item: Non-sterile Recalled by SVS LLC Due to Mislabeling

The Issue: Firm received complaints regarding skin irritation when using the gloves,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...

The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...

The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...

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

Class II — Potential Health HazardOngoing