Walgreens Recalls Pedi MVI Syringes Due to Sterility Concerns
Walgreens Infusion Services is recalling 73 syringes of Pedi MVI in Texas due to a lack of assurance of sterility.
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, which corresponds to a Severe rating under the rubric, particularly given the risk of infection from non-sterile medical products.
Plain-English summary
Walgreens Infusion Services is recalling 73 syringes of Pedi MVI, a prescription-only medication compounded by Option Care 148 in San Antonio, Texas. The recall was initiated because of a lack of assurance of sterility in the product.
The affected product is distributed in Texas. The recall covers all lots within their expiry dates. No specific lot numbers or dates are provided in the source text.
Consumers who have this product should stop using it and contact their healthcare provider or pharmacist for further instructions.
The recalled product
- Product
- Pedi MVI a) 5 mL, b) 10 mL syringe, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
- Manufacturer
- Walgreens Infusion Services
- Category
- Drug — Compounded Medication
- Affected units
- 73
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 (1)
- All lots within expiry.
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 33 recalled by Walgreens Infusion Services 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.
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