CLASS II Drug recall · Reported 30 Mar 2022 · FDA Enforcement Report

Sermorelin Acetate Lyophilized powder for reconstitution recalled

Olympia Compounding Pharmacy is recalling Sermorelin Acetate Lyophilized powder for reconstitution, Multi-Dose 9 mg per vial, Each, distributed nationwide in the US. The recall was initiated on 8 Mar 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots: D44026 Exp. 4/26/22; F42104 Exp. 6/4/22
Quantity recalled2283 vials

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-0718-2022
FDA event ID
89717
Recalling firm
Olympia Compounding Pharmacy, Orlando, FL
Classification
Class II
Status
Terminated
Recall initiated
8 Mar 2022
FDA classified
29 Mar 2022
Reported
30 Mar 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

8 Mar 2022Recall initiated by company
29 Mar 2022Classified by FDA+21 days
30 Mar 2022Published in enforcement report+1 day

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Sub Potent

Product as listed by the FDA

Sermorelin Acetate Lyophilized powder for reconstitution, Multi-Dose 9 mg per vial, Each ML contains: 5% Mannitol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0059-00

Where it was distributed

Nationwide in the USA including Puerto Rico.

Nationwide Puerto Rico

Questions about this recall

Why was it recalled?

Sub Potent

Which lots are affected?

Lots: D44026 Exp. 4/26/22; F42104 Exp. 6/4/22

Where was it sold?

Nationwide in the USA including 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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

6 other products · FDA event 89717

More recalls from Olympia Compounding Pharmacy

All 94

Other Sermorelin Lyophilized For Reconstitution recalls

All 2
ReportedClassRecallCompanyReasonWhere
DrugCLASS IISermorelin Lyophilized powder for reconstitution, 10mg recalledGenoGenixSterilityNationwide