Healix Infusion Therapy, Inc.: 6 recalls on record

Recalls filed with 1 agency: FDA (6).

First recall on record: July 16, 2014. Most recent: August 27, 2014.

Risk classification: Class II: 6

Most recent recalls

DateAgencyProduct
August 27, 2014FDAfentaNYL 2750 mcg/55 mL (50 mcg/mL) in prefilled syringe, COMPOUNDED DRUG, For Institut…D-1554-2014
August 27, 2014FDAfentaNYL 200 mcg/100 mL (2 mcg/mL) and Ropivacaine 0.2% in 0.9% Sodium Chloride 100mL, in…D-1553-2014
August 27, 2014FDAfentaNYL 5000 mcg/250 mL (20 mcg/mL) in 0.9% Sodium Chloride in a flexable bag, COMPOUNDE…D-1555-2014
August 27, 2014FDAfentaNYL 1500 mcg/30 mL (50 mcg/mL) in prefilled syringe, COMPOUNDED DRUG For Institut…D-1551-2014
August 27, 2014FDAfentaNYL 2500 mcg/250 mL (10 mcg/mL) in 0.9% Sodium Chloride in flexable bag, COMPOUNDED …D-1552-2014
July 16, 2014FDABUPivacaine HCl 0.25% Preservative Free (2.5 mg/mL) 500 mL in On-Q C-bloc (2-14 mL/hr) ba…D-1422-2014

Questions about this company

How many recalls does Healix Infusion Therapy, Inc. have?
Recalert has 6 U.S. recalls on record for Healix Infusion Therapy, Inc., published between July 16, 2014 and August 27, 2014.
What was the most recent Healix Infusion Therapy, Inc. recall?
FDA recall D-1554-2014, published August 27, 2014: fentaNYL 2750 mcg/55 mL (50 mcg/mL) in prefilled syringe, COMPOUNDED DRUG, For Institutional or Office Use Only--Not for Resale Federal Law Prohibits Dispensing without Prescription Healix Infus…
Which agencies have handled Healix Infusion Therapy, Inc. recalls?
Healix Infusion Therapy, Inc. appears as the recalling firm in recalls from: FDA (6).

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