The Recall Desk
SevereFDA (Drugs)·D-1473-2014·Announced 2014-07-30

Trinity Care Solutions Recalls Vancomycin Due to Sterility Concerns

Trinity Care Solutions is recalling 14 units of Vancomycin 1.25 gm/250 mL due to lack of assurance of sterility identified during an FDA inspection.

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 recall is classified as FDA Class II and involves a lack of assurance of sterility in a parenteral product, which poses a significant risk of serious injury or death from infection, meeting the criteria for a Severe rating.

Plain-English summary

Trinity Care Solutions, operating as Franck's Lab Inc, is recalling 14 units of Vancomycin 1.25 gm/250 mL 0.9%NS. The product is labeled for parenteral use only and was distributed in Florida. The specific recall number is D-1473-2014.

The recall was initiated due to a lack of assurance of sterility. This decision follows concerns regarding quality control procedures observed during a recent FDA inspection. The agency has classified this recall as Class II.

All lots of sterile products compounded by the pharmacy within their expiry dates are subject to this recall. Patients and healthcare providers should stop using the affected product and contact their pharmacist or healthcare provider for further instructions.

The recalled product

Product
Vancomycin 1.25 gm/250 mL 0.9%NS,Trinity Care Solutions, 202-C SW 17th Street, Ocala, FL 34471-5138, For Parenteral Use Only, Rx # 29140, Discard After 05/23/14
Affected units
14

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)

  • Rx # 29140
  • Exp 05/23/14

Distribution

Distributed in 1 state:

Part of a larger recall action

This product is one of 30 recalled by Franck's Lab Inc dba Trinity Care Solutions 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 30 products in this recall →