Fresh Recalls

FDANot Yet Classified · Drug · FDA event 99666; recall number pending · Recalled September 2, 2026

Ibuprofen recall — Safecor Health, LLC

Agency report date: September 2, 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
Ibuprofen
Company / brand
Safecor Health
Lot / serial / date codes
Lot #: 26281630, Exp. Date 1/27/2027
Distribution
MA only
Agency product description and boundaries

Ibuprofen, 150 mg per 7.5 mL, Delivers: 7.5 mL, Conc: 20 mg/mL, Oral Suspension, 12mL Oral Syringes, Berry Flavor/Alcohol Free, Mfg By: MCNEIL, Pkg by: Safecor, Woburn, MA

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: Cross Contamination with Other Products

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

Affected product: Ibuprofen recall status

3. Open the official notice or contact

Official recall ID
Not yet assigned by the FDA — identified by FDA event ID 99666
Brand
All Safecor Health recalls
Classification
Not Yet Classified
Units affected
302 syringes
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Woburn, MA, United States
Firm address
317 New Boston St, N/A, 01801-6231

Identifying details (verbatim from the notice)

Product codes / lots
Lot #: 26281630, Exp. Date 1/27/2027
Distribution
MA only
Firm notified the public via
Letter
FDA event ID
99666
Recall initiated
August 14, 2026
FDA report date
September 2, 2026

Other drug recalls from around the same time

Verify with the official sources:

Found something wrong or missing? Report a data error.

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 September 29, 2026 at 12:00 AM UTC.

Report a data error on this page