August 2026 FDA Recall Drug by Safecor Health, Llc
N/A - Cross Contamination with Other Products

This Not Yet Classified drug recall was voluntarily initiated by Safecor Health, Llc on August 14, 2026 for the product Drug. The FDA reported the reason for recall as cross contamination with other products. The product was distributed in MA only and the recall is currently ongoing.

Recall Number: N/A

Reason for Recall
Cross Contamination with Other Products
Initiated
08-14-2026
Reported
09-02-2026
Quantity
302 syringes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
99666
Classification About Classification
Relative degree of health hazard assigned by FDA.
Not Yet Classified
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Ongoing
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Safecor Health, LLC
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
MA only
Product Description About Product Description
Full technical description of the product.
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

Batch or Lot Expiration Information

Lot# : 26281630, Exp. Date 1/27/2027