The Recall Desk
SevereFDA (Drugs)·D-1169-2016·Announced 2016-07-20

Medaus Recalls B-Complex Vials Due to Sterility Assurance Concerns

Medaus, Inc. is recalling B-Complex (Lieberman) in NaCl 0.9% (PF) 2 mL vials due to a lack of assurance of sterility. The product was 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. Per the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), particularly when involving potential hospitalization or significant injury risks associated with sterility failures in injectable products.

Plain-English summary

Medaus, Inc. is recalling B-Complex (Lieberman) in NaCl 0.9% (PF), 2 mL vials, manufactured by Medaus Pharmacy. The recall is being conducted due to a lack of assurance of sterility. The affected product is identified by Lot # 151229-15 with a beyond-use date of 06/26/16.

The recalled product was distributed in the United States, Japan, and New Zealand. The FDA has classified this recall as Class II, which indicates 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 product and contact Medaus, Inc. for further instructions or a replacement. No specific instructions for disposal or return are provided in the source text.

The recalled product

Product
B-COMPLEX (LIEBERMAN) IN NACL 0.9% (PF), B1-12.5MG, B2-5-PO4-10MG, B3-12.5MG, B5-12.5MG, B6-12.5MG/ML, 2ML 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 (2)

  • Lot #: 151229-15
  • BUD: 06/26/16

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 →

Related recalls

Same manufacturer · Medaus, Inc.

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Same hazard · sterility failure

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