CLASS II Drug recall · Reported 1 Jun 2022 · FDA Enforcement Report
Olympia Mineral Blend Magnesium Chloride 80 mg/mL Zinc recalled
Olympia Compounding Pharmacy is recalling Olympia Mineral Blend Magnesium Chloride 80 mg/mL Zinc Sulfate 1 mg/mL Manganese Sulfate, distributed nationwide in the US. The recall was initiated on 9 May 2022 and the FDA has classified it as Class II.
Check your package
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-0941-2022
- FDA event ID
- 90204
- Recalling firm
- Olympia Compounding Pharmacy, Orlando, FL
- Classification
- Class II
- Status
- Completed
- Recall initiated
- 9 May 2022
- FDA classified
- 25 May 2022
- Reported
- 1 Jun 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Drug class
- Injectable & IV Drugs
Timeline
| 9 May 2022 | Recall initiated by company | |
| 25 May 2022 | Classified by FDA | +16 days |
| 1 Jun 2022 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of assurance of sterility.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Olympia Mineral Blend Magnesium Chloride 80 mg/mL Zinc Sulfate 1 mg/mL Manganese Sulfate 20 mcg/mL Copper Gluconate 0.2 mg/mL Sodium Selenite 18 mcg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0061-30.
Where it was distributed
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands
Questions about this recall
Why was it recalled?
Lack of assurance of sterility.
Which lots are affected?
Lots: L24B1 BUD: 6/16/2022, L24D16 BUDL 6/16/2022, A24C24-22, A24E24-22 BUDL 7/24/2022
Where was it sold?
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands
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
52 other products · FDA event 90204This product is part of a recall event; the main page for the event is Sodium Bicarbonate 8.4% MDV Injection, Multi-Dose vial recalled.
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