CLASS II Drug recall · Reported 17 Nov 2021 · FDA Enforcement Report
Blue Tree Lipo Extreme (/w Methylcobalamin) Injection Injectable recalled
Vita Pharmacy is recalling Blue Tree Lipo Extreme (/w Methylcobalamin) Injection Injectable, distributed in Puerto Rico, Washington. The recall was initiated on 12 Oct 2021 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0108-2022
- FDA event ID
- 88862
- Recalling firm
- Vita Pharmacy, San Antonio, TX
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Oct 2021
- FDA classified
- 8 Nov 2021
- Reported
- 17 Nov 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Sterility
- Drug class
- Injectable & IV Drugs
Timeline
| 12 Oct 2021 | Recall initiated by company | |
| 8 Nov 2021 | Classified by FDA | +27 days |
| 17 Nov 2021 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of assurance of sterility
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
BLUE TREE LIPO EXTREME (/W METHYLCOBALAMIN) INJECTION INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
Where it was distributed
United States including Washington, D.C. and Puerto Rico
Questions about this recall
Is Blue Tree Lipo Extreme (/w Methylcobalamin) Injection Injectable recalled?
Yes. Vita Pharmacy recalled Blue Tree Lipo Extreme (/w Methylcobalamin) Injection Injectable on 12 Oct 2021. The recall is Class II and its status is Terminated. Recall number D-0108-2022.
Why was it recalled?
Lack of assurance of sterility
Which lots are affected?
Lot: 09172021:87 BUD: 12/16/2021
Where was it sold?
United States including Washington, D.C. and Puerto Rico
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Vita Pharmacy
All 130| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Tri-mix Papaverine 30/phentolamine 2/pge-1 30 Inj Injectable recalled | Vita Pharmacy | Sterility | PR, WA |
| Drug | CLASS II | Alprostadil 25mcg/ML 25mcg/ML Injectable recalled by Vita Pharmacy | Vita Pharmacy | Sterility | PR, WA |
| Drug | CLASS II | Testosterone Bi-blend 100/100mg/ML Injectable recalled by Vita Pharmacy | Vita Pharmacy | Sterility | PR, WA |
| Drug | CLASS II | Alprostadil 32mcg/ML 32mcg/ML Injectable recalled by Vita Pharmacy | Vita Pharmacy | Sterility | PR, WA |
| Drug | CLASS II | Alprostadil 30mcg/ML Inj 30mcg/ML Injectable recalled by Vita Pharmacy | Vita Pharmacy | Sterility | PR, WA |