The Recall Desk
SevereFDA (Drugs)·D-0212-2019·Announced 2018-11-07

Pharm D Solutions Recalls Zinc Sulfate Injectable Due to Sterility Concerns

Pharm 184 vials of Zinc Sulfate 1 mg/mL MDV Injectable are being recalled nationwide 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 and involves a lack of assurance of sterility in an injectable product, which poses a significant risk of infection or serious injury.

Plain-English summary

Pharm D Solutions, LLC is recalling 184 vials of Zinc Sulfate 1 mg/mL MDV Injectable (NDC 69699-1418-10). The recall is being conducted because of a lack of assurance of sterility for the product.

The affected product is identified by Lot 06072018:60, with a discard by date of 12/4/2018. The recall is classified as Class II by the FDA.

The product was distributed nationwide. Consumers and healthcare providers should check their inventory for this specific lot and date, and discontinue use if found.

The recalled product

Product
Zinc Sulfate 1 mg/mL MDV Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1418-10
Manufacturer
Pharm D Solutions, LLC
Category
Drug — Injectable
Hazard
Affected units
184

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)

  • Lot: 06072018:60 Discard by: 12/4/2018

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 79 recalled by Pharm D Solutions, LLC 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 79 products in this recall →

Related recalls

Same manufacturer · Pharm D Solutions, LLC

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Same hazard · sterility

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