The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-0646-2018·Announced 2018-04-25

Partell Specialty Pharmacy Recalls Vitamin D Injectable Due to Sterility Concerns

Partell Specialty Pharmacy is recalling Vitamin D 50,000 unit/ml injectable liquid because it was sterilized using a non-approved method.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. 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 the hazard involves a lack of assurance of sterility in an injectable drug, which poses a significant risk of infection or serious injury.

Plain-English summary

Partell Specialty Pharmacy is recalling 4 vials of Vitamin D 50,000 unit/ml, 5 mL amber vial, Injectable Liquid. The recall is due to a lack of assurance of sterility, as the firm used a non-approved method of sterilization for the drug products.

The affected products are prescription-only (Rx only) and were distributed only in Nevada. Specific lot numbers and best-use dates are listed in the recall documentation, including lots 20180220@4, 20180221@14, and 20180228@1.

Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for further instructions.

The recalled product

Product
Vitamin D 50,000 unit/ml, 5 mL amber vial, Injectable Liquid, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. # 101, Las Vegas, NV 89119 (702) 791-3800
Manufacturer
Partell Specialty Pharmacy
Category
Drug — Injectable
Hazard
Affected units
4

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 (6)

  • Lot#: 20180220@4
  • BUD 03/22/2018
  • 20180221@14
  • BUD 03/23/2018
  • 20180228@1
  • BUD 03/30/2018.

Distribution

Distributed in 1 state:

Part of a larger recall action

This product is one of 49 recalled by Partell Specialty Pharmacy 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 49 products in this recall →

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