Healix Infusion Therapy recalls
Healix Infusion Therapy has 6 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 27 Aug 2014. The most frequent reason is sterility.
Total recalls6since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 27 Aug 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 6 100%Class III 0 0%
Why healix infusion therapy is recalled
Product types
By year
All healix infusion therapy recalls, newest first
6 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | fentaNYL 200 mcg/ (2 mcg/mL) and Ropivacaine recalled | Healix Infusion Therapy | Sterility | GA, TX |
| Drug | CLASS II | fentaNYL 2750 mcg/ (50 mcg/mL) in prefilled syringe recalled | Healix Infusion Therapy | Sterility | GA, TX |
| Drug | CLASS II | fentaNYL 2500 mcg/ (10 mcg/mL) in 9% Sodium Chloride recalled | Healix Infusion Therapy | Sterility | GA, TX |
| Drug | CLASS II | fentaNYL 1500 mcg/ (50 mcg/mL) in prefilled syringe recalled | Healix Infusion Therapy | Sterility | GA, TX |
| Drug | CLASS II | fentaNYL 5000 mcg/ (20 mcg/mL) in 9% Sodium Chloride recalled | Healix Infusion Therapy | Sterility | GA, TX |
| Drug | CLASS II | BUPivacaine HCl 25% Preservative Free 5 mg/mL) recalled | Healix Infusion Therapy | Particulate Matter | TX |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.