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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 91707

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 14, 2023
Product types
Drug
Classifications
Class I and Class II
Statuses
Ongoing
Recalling firm wording
Pharmedica USA, LLC

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 2

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.

D-0456-2023
Recall number
D-0456-2023
Initiated
February 14, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Pharmedica USA, LLC
Quantity
a) 869 bottles; b) 1035 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Non-Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-Sterility

Code information

Lot #s: a) 1808051, Exp.: 01/01/2027; b) 2203PS01, Exp.: 01/01/2027

Distribution pattern

Nationwide in the USA and Worldwide through e-commerce and trade shows

drug · product 2 of 2

Purely Soothing MSM Nasal Spray, 15%, packaged in 30ml, 1.014 fl. oz bottles, Manufactured by: Pharmedica USA, Phoenix, AZ, UPC 7 31034 91380 5

D-0457-2023
Recall number
D-0457-2023
Initiated
February 14, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Pharmedica USA, LLC
Quantity
995 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations

Code information

Lot #: 1808051, Exp.: 01/01/2027

Distribution pattern

Nationwide in the USA and Worldwide through e-commerce and trade shows