The Recall Desk
SevereFDA (Drugs)·D-1259-2019·Announced 2019-05-08

Customceutical Compounding Recalls Test D Vials Due to Sterility Concerns

Customceutical Compounding is recalling Test D vials because the manufacturer cannot ensure the injectable solution is sterile.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a Severe severity score under the rubric for drug recalls involving potential serious health consequences.

Plain-English summary

Customceutical Compounding is recalling 2 vials of Test D (Testosterone Cypionate 200mg/ml Vitamin D3 5,000IU/ml), 5 ml multidose vials. The recall is due to a lack of assurance of sterility for the injectable solution.

The affected product is identified by Lot # 03132019@28 and has an expiration date of 6/11/19. The product was distributed nationwide in the U.S.A.

Consumers should stop using the product and contact the recalling firm, Customceutical Compounding, located at 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028, or by phone at 480 516 0272, for further instructions.

The recalled product

Product
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
Hazard
Affected units
2

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot #: 03132019@28
  • Exp 6/11/19

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 10 recalled by Customceutical Compounding under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 10 products in this recall →