The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-0182-2019·Announced 2018-11-07

Pharm D Solutions Recalls Sermorelin/GHRP-2 Powder Due to Sterility Concerns

Pharm D Solutions is recalling 330 vials of Sermorelin/GHRP-2 Powder because the company cannot ensure the product is sterile.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. 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. According to the rubric, an FDA Class II recall involving a sterile product defect (which carries a risk of serious infection) falls under the 'Severe' category, particularly given the lack of assurance of sterility for an injectable powder.

Plain-English summary

Pharm D Solutions, LLC is recalling 330 vials of Sermorelin/GHRP-2 9 mg-6 mg Powder (NDC 69699-1728-10). The recall was initiated because the company lacks assurance of the product's sterility.

The affected product was distributed nationwide. The recall covers two specific lots: Lot 03202018:06 with a discard by date of 9/16/2018, and Lot 06112018:49 with a discard by date of 12/8/2018.

Consumers and healthcare providers should stop using the recalled product and contact Pharm D Solutions, LLC or their healthcare provider for further instructions.

The recalled product

Product
Sermorelin/GHRP-2 9 mg-6 mg Powder, Pharm D Solutions, Houston, Texas --- NDC 69699-1728-10
Manufacturer
Pharm D Solutions, LLC
Category
Drug — Injectable Powder
Hazard
Affected units
330

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: 03202018:06 Discard by: 9/16/2018
  • 06112018:49 Discard by: 12/8/2018

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 79 recalled by Pharm D Solutions, LLC 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 79 products in this recall →

Related recalls

Same manufacturer · Pharm D Solutions, LLC

See all →

Same hazard · lack of sterility

See all →

Similar recalls