RECALL ALERT~ 600,000 Ventolin Rescue Inhalers This is a CLASS II Recall Meaning It Could Cause a Temporary Health Crisis! Please Read & Share This Information!

OH NO You could have a SERIOUS Problem with your Ventolin Rescue Inhaler!

ventolin

This is a NEW RECALL The Recall Initiation Date is 3/22/2017.

This Recall is on Ventiolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, net weight 18 g inhalers, RX only.

Reason for Recall:

Defective Delivery System: Elevated number of units with out of specification results for leak rate.

D-0626-2017

Code Information:

Lot #: 6ZP9848, Exp 03/18; 6ZP0003, 6ZP9944, Exp 04/18.

Classification:

Class II

If patients have questions regarding a Ventolin HFA unit, or wish to know if their inhaler is included in the recall, they may contact GSK’s Customer Service Center at 1-888-825-5249, Monday-Friday, 8:30 am – 5:30 pm ET. If a patient believes his or her Ventolin HFA inhaler is not effective at relieving his or her symptoms, the patient should seek immediate medical attention from his or her healthcare provider.

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RECALL ALERT – Do You or Someone You Know Use Ventolin? Then You MUST Read This – PLEASE SHARE

ventolin

 

 

GlaxoSmithKline voluntary recall of Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations

Even though this recall was from December, I felt it was important to still make everyone aware. Some may still have these laying around

 

Product Description Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Rx Only, For Oral Inhalation Only, Net Wt. 18 g, GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0682-20
Recall Number D-0519-2016
Classification Class II
Code Info Lot #s: 5ZP1708, Exp. 12/2016; 5ZP1951, Exp. 02/2017
Product Distributed Qty 128,704 Inhalers
Reason For Recall Defective Delivery System: Some canisters may not contain sufficient propellant to deliver the labeled claim of 200 actuations through the end of shelf life.

 

The voluntary retail-level recall affects only two lots of Ventolin HFA, in the US. The recall does not extend beyond the US. The lot numbers are 5ZP1708 and 5ZP1951, which were distributed only in the US market. Please note that lot number 5ZP1708 was manufactured on 07 July 2015, with an expiry date of December 2016. Lot 5ZP1951 was manufactured on 22 August 2015 with an expiry date of February 2017.

No other lots are affected by the voluntary recall, meaning that, regardless of expiration date or doses indicated in dose counters, only inhalers in these two lots are affected.

People with inhalers that match the expiration date on the Ventolin HFA inhaler, but not the lot number, are not impacted by the recall.

If patients have questions regarding a Ventolin HFA unit, or wish to know if their inhaler is included in the recall, they may contact GSK’s Customer Service Center at 1-888-825-5249, Monday-Friday, 8:30 am – 5:30 pm ET. If a patient believes his or her Ventolin HFA inhaler is not effective at relieving his or her symptoms, the patient should seek immediate medical attention from his or her healthcare provider.”

 

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