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Recall of Inhalers

Nearly 600,000 inhalers were just voluntarily recalled nationwide by GlaxoSmithKline due to "defective delivery system," with a large number of units having "out of specification results for leak rate" (possible package leakage).

The FDA describes the affected inhalers as prescription-only "Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, net weight 18 g inhalers." The recall is classified as "Class II," which means "the products might cause a temporary health problem, or pose only a slight threat of a serious nature," the FDA reports.

To see if your child's inhaler is affected by this recall, see the lot numbers and expiration dates of the affected inhalers below.

  • 6ZP9848 (expiration date: March 2018)
  • 6ZP0003 (expiration date: April 2018)
  • 6ZP9944 (expiration date: April 2018)
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