Customceutical Compounding recalls BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV INJ
Customceutical Compounding recalls BPlex injectable vials due to lack of sterility assurance. Affected vials contain methylcobalamin, pyridoxal phosphate, and dexpantenol. No remedy specified in official notice.
Recall notice
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Contact the company & request your remedy
What happened, in plain English
Customceutical Compounding has recalled BPlex injectable vials because they may not be sterile. This poses a risk of infection if used improperly. The recall affects vials with specific lot numbers sold in Phoenix, Arizona. Read more at govinfonow.com/recall/38945-customceutical-bplex-injectable-recall-sterility-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/38945-customceutical-bplex-injectable-recall-sterility-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1254-2019
Cite this page
“Customceutical BPlex Injectable Recall: Sterility Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38945-customceutical-bplex-injectable-recall-sterility-risk. Based on FDA recall #D-1254-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1254-2019%22&limit=1).
Why it’s dangerous
The vials lack proper sterility assurance, meaning they could become contaminated with bacteria. If injected, this could lead to infections or other health issues. The risk is specific to injectable products meant to be sterile.
Who’s affected
People who received BPlex vials compounded by Customceutical Compounding in Phoenix, Arizona. Those using the product for medical injections are most at risk.
How to tell if you have this one
Check for the lot number 03122019@31 on the vial label. The vials were compounded by Customceutical Compounding in Phoenix, Arizona and expire June 10, 2019.
- Brand
Customceutical Compounding- Category
Drug
All 10 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
U.S.A. Nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1253-2019 | BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 02082019@9, Exp 5/19/19 | 32 vials |
| D-1254-2019 | BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 03122019@31, Exp 6/10/19 | 19 vials |
| D-1255-2019 | Glutathione 200mg/mL inj. a) 10 ML and b) 12 ML MULTIDOSE VIAL MDV Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 02132019@25, Exp 5/14/19 | 4 vials |
| D-1256-2019 | HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 5 mL multidose vial compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 03132019@23, Exp 5/12/19 | 12 vials |
| D-1257-2019 | Lipoplex (METHIONINE 25 MG/ML INOSITOL 50 MG/ML CHOLINE CHLORIDE 50 MG/ML HYDROXOCOBALAMIN 500 MC/ML DEXPANTHENOL 50 MG/ML PYRIDOXINE HCL 50 MG/ML), 10 ML MULTIDOSE VIAL INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 02212019@13, Exp 5/22/19 | 16 vials |
| D-1258-2019 | Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5,000IU/ML), 5 ML MULTIDOSE VIAL COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 01232019@25, Exp 4/23/19 | 8 vials |
| D-1259-2019 | Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5,000IU/ML), 5 ML MULTIDOSE VIAL COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 03132019@28, Exp 6/11/19 | 2 vials |
| D-1260-2019 | Test PROCYP (TESTOSTERONE CYPIONATE 200MG/ML TESTOSTERONE PROPIONATE 20MG/ML), 5 ML MULTIDOSE VIAL INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 03112019@10, Exp 6/19/19 | 5 vials |
| D-1261-2019 | Trimix HIGH (Papaverine HCl 30 mg/mL Phentolamine Mesylate 2 mg/mL Alprostadil 20 mcg/mL), 2 mL multidose vial MDV Inj. Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 02182019@27, Exp 8/02/19 | 3 vials |
| D-1262-2019 | TriMix MEDIUM (Papaverine HCL 21 mg/mL Phentolamine Mesylate 0.7 mg/mL Alprostadil 7 mcg/mL), 2 mL multidose MDV Inj. Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272; Lot #: 02182019@22, Exp 8/02/19 | N/A |
What to do — step by step
Check Vial Label
Look for the lot number 03122019@31 on the vial label to confirm if it's affected.
Questions people ask
Is there a fix for this issue?
The official recall notice does not specify any remedy.
How can I tell if I have the recalled product?
Check for the lot number 03122019@31 on the vial label. The vials were compounded by Customceutical Compounding in Phoenix, Arizona and expire June 10, 2019.
What should I do if I have the recalled vial?
The official recall notice does not specify any remedy.
Contact Customceutical Compounding
We’ve drafted a message you can send Customceutical Compounding to request your refund or repair — edit it as you like.
Subject: Recall D-1254-2019 — Customceutical Compounding Customceutical Compounding Hello, I own a Customceutical Compounding that is covered by recall D-1254-2019 from Customceutical Compounding. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1254-2019 (April 8, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1254-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.