The Recall Desk
SevereFDA (Drugs)·D-1198-2016·Announced 2016-07-20

Medaus Recalls L-Glutathione Vials Due to Sterility Concerns

Medaus, Inc. is recalling L-Glutathione 100mg/mL vials because the product lacks assurance of sterility. The recall covers vials distributed in the U.S., Japan, and New Zealand.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The FDA classified this recall as Class II. According to the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), particularly when the hazard involves sterility assurance which carries a risk of infection.

Plain-English summary

Medaus, Inc. is recalling L-Glutathione 100mg/mL (PF) 10 mL vials due to a lack of assurance of sterility. The affected product is identified by Lot # 160222-28 with a best use date of 05/22/16, and Lot # 160302-63 with a best use date of 05/31/16. The total quantity involved is 5,000 mL in vials.

The recall covers product distributed nationwide in the United States, as well as in Japan and New Zealand. The FDA has classified this recall as Class II, indicating that use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Consumers and healthcare providers should stop using the affected vials and contact Medaus, Inc. for further instructions or a refund. The source text does not report any specific illnesses or injuries associated with this recall.

The recalled product

Product
L-GLUTATHIONE 100MG/ML (PF), 10 ML Vials, MEDAUS PHARMACY
Manufacturer
Medaus, Inc.
Category
Drug — Injectable
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • Lot #: 160222-28
  • BUD: 05/22/16
  • Lot #: 160302-63
  • BUD: 05/31/16

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 88 recalled by Medaus, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 88 products in this recall →

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