CLASS I ONGOING Drug recall · Reported 15 Mar 2023 · FDA Enforcement Report
Purely Soothing 15% MSM Drops recalled by Pharmedica USA
Pharmedica USA is recalling Purely Soothing 15% MSM Drops, distributed nationwide in the US. The recall was initiated on 14 Feb 2023 and the FDA has classified it as Class I.
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-0456-2023
- FDA event ID
- 91707
- Recalling firm
- Pharmedica USA, Phoenix, AZ
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 14 Feb 2023
- FDA classified
- 10 Mar 2023
- Reported
- 15 Mar 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Sterility
Timeline
| 14 Feb 2023 | Recall initiated by company | |
| 10 Mar 2023 | Classified by FDA | +24 days |
| 15 Mar 2023 | Published in enforcement report | +5 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Non-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
Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manufactured by: Pharmedica USA, Phoenix, AZ.
Where it was distributed
Nationwide in the USA and Worldwide through e-commerce and trade shows
Stores named: Online Retailers
Questions about this recall
Why was it recalled?
Non-Sterility
Which lots are affected?
Lot #s: a) 1808051, Exp.: 01/01/2027; b) 2203PS01, Exp.: 01/01/2027
Where was it sold?
Nationwide in the USA and Worldwide through e-commerce and trade shows
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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
1 other product · FDA event 91707| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Purely Soothing MSM Nasal Spray recalled by Pharmedica USA | Pharmedica USA | Manufacturing (CGMP) Deviations | Nationwide |
More recalls from Pharmedica USA
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Purely Soothing MSM Nasal Spray recalled by Pharmedica USA | Pharmedica USA | Manufacturing (CGMP) Deviations | Nationwide |
Other Purely Soothing Msm recalls
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Purely Soothing MSM Nasal Spray recalled by Pharmedica USA | Pharmedica USA | Manufacturing (CGMP) Deviations | Nationwide |