Safety

Product Photos

  • Product labeling Enovachem Pharmaceuticals Dyural-40
  • Product labeling Enovachem Pharmaceuticals Dyural-80

Announcement

Torrance, CA, Asclemed USA Inc is voluntarily recalling 20 lots of Dyural-40 and 61 lots of Dyural-80, to the user level. The products include recalled Sodium Chloride, USP, 0.9% manufactured by Fresenius Kabi, which has been recalled due to product labeling incorrectly stating stoppers do not contain latex.

For the population most at risk, those with a severe allergic reaction to latex, there is probability of an anaphylactic reaction, and this could result in hospitalization or death. To date, Asclemed USA Inc has not received any reports of adverse events related to this recall.

The products are Dyural-40 convenience kits packaged in plastic trays and Dyural-80 convenience kits packaged in plastic trays, containing Sodium Chloride, USP, 0.9% by Fresenius Kabi.

The affected Dyural-40 lots include the following:

LOTEXPLOTEXPLOTEXPLOTEXP
051518X51/31/2019072518X35/31/2019090518X46/30/2019092418X18/31/2019
051618X11/31/2019072718X15/31/2019091818X21/31/2019092818X48/31/2019
052318X45/1/2019080318X25/31/2019091818X37/31/2019101018X38/31/2019
052318X55/31/2019082318X46/30/2019091818X46/30/2019101018X58/31/2019
062818X15/31/2019083118X16/30/2019091818X58/31/2019102418X59/30/2019

The affected Dyural-80 lots include the following:

LOTEXPLOTEXPLOTEXPLOTEXP
050918X112/31/2018062718X16/30/2019080718X76/30/2019100518X67/31/2019
051518X45/31/2019062718X26/30/2019080918X36/30/2019101118X37/31/2019
051618X1012/31/2018062818X36/30/2019083018X26/30/2019101518X27/31/2019
051818X412/31/2018062818X46/30/2019083118X26/30/2019101618X77/31/2019
051818X55/31/2019070918X16/30/2019083118X56/30/2019101618X87/31/2019
052118X45/31/2019071018X56/30/2019090518X56/30/2019101818X37/31/2019
052118X55/31/2019071118X46/30/2019090518X67/31/2019101918X17/31/2019
052918X75/31/2019071118X56/30/2019090718X27/31/2019102318X17/31/2019
061118X85/1/2019071718X22/28/2019090718X37/31/2019103118X17/31/2019
061118X95/31/2019072018X66/30/2019090718X57/31/2019103118X27/31/2019
061118X105/31/2019072418X36/30/2019091118X77/31/2019103118X39/30/2019
061418X25/31/2019072418X46/30/2019091318X57/31/2019110618X19/30/2019
061518X15/31/2019072518X26/30/2019091918X17/31/2019110818X19/30/2019
061518X26/30/2019073018X46/30/2019092718X17/31/2019
061918X26/30/2019073018X86/30/2019092718X27/31/2019
062518X26/30/2019080218X36/30/2019092818X37/31/2019

The products can be identified by lot and expiration stamped on the front of each convenience kit. Product was distributed Nationwide to distributors and physicians.

Asclemed USA Inc is notifying its distributors and customers by email and is arranging for return of all recalled products. Distributors and physicians that have Dyural-40 or Dyural-80 which is being recalled should stop using them and return to place of purchase.

Consumers with questions regarding this recall can contact Asclemed USA Inc by calling (310) 320-0100 ext. 120 Monday through Friday from 7:30am to 4:00pm PST or emailing christinah@enovachem.us.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

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