The Recall Desk
SevereFDA (Drugs)·D-1058-2015·Announced 2015-05-20

Health Innovations Pharmacy Recalls Triest and Progest Capsules for Sterility Concerns

Health Innovations Pharmacy is recalling Triest 5 mg - Progest 150 mg capsules due to lack of assurance of sterility and stability data.

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 agency classification is FDA Class II. According to the rubric, FDA Class II recalls involving significant risks such as sterility issues are classified as Severe (Score 4), as they are not Class I but involve potential serious health consequences.

Plain-English summary

Health Innovations Pharmacy, Inc. is recalling Triest 5 mg - Progest 150 mg Capsules. The recall was initiated because recent inspection observations associated with certain quality control procedures present a risk to sterility and quality assurance.

The source text indicates that the lack of assurance of sterility and stability data does not support the product's expiry. The recall applies to all lots of the product. Distribution was limited to North Carolina.

Consumers who have this product should stop using it and contact Health Innovations Pharmacy at (910) 246-5155 for further instructions.

The recalled product

Product
Triest 5 mg - Progest 150 mg Capsule, Health Innov Pharmacy, 295 Pinehurst Ave, Southern Pines, NC 28387, (910) 246-5155

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 (1)

  • All lots

Distribution

Distributed in 1 state:

Part of a larger recall action

This product is one of 65 recalled by Health Innovations Pharmacy, Inc 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 65 products in this recall →