Fresh Recalls

FDAClass II · Drug · Recall D-0861-2026 · Recalled September 30, 2026

Major LubriFresh P recall — Sterling Pharmaceutical Services LLC

Agency report date: September 30, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Major LubriFresh P
Company / brand
Sterling Pharmaceutical Services
Lot / serial / date codes
Lot # 3183
Distribution
USA Nationwide
Agency product description and boundaries

Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Lack of Assurance of Sterility

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Major LubriFresh P recall status

3. Open the official notice or contact

Official recall ID
D-0861-2026
Brand
All Sterling Pharmaceutical Services recalls
Classification
Class II
Units affected
34368 tubes
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Dupo, IL, United States
Firm address
109 S 2nd St, 62239-1351

Identifying details (verbatim from the notice)

Product codes / lots
Lot # 3183
Distribution
USA Nationwide
Firm notified the public via
Letter
FDA event ID
99712
Recall initiated
August 20, 2026
FDA classified
September 21, 2026
FDA report date
September 30, 2026

Other drug recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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