The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-0074-2020·Announced 2019-10-09

KRS Global Biotechnology Recalls IV Magnesium and Calcium Vials for Sterility Concerns

KRS Global Biotechnology is recalling 878 vials of IV magnesium and calcium solution due to a lack of assurance of sterility.

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 involves a lack of assurance of sterility in an intravenous product, which poses a significant risk of serious injury or death if contaminated.

Plain-English summary

KRS Global Biotechnology, Inc. is recalling 878 vials of Magnesium Chloride Hexahydrate 82.5 mg/mL; Calcium Gluconate 30 mg/mL (PF), For IV Use, 10 mL Single Dose vials. The product is identified by NDC 3321678355. The recall is being conducted because of a lack of assurance of sterility.

The affected product was distributed nationwide. All lots remaining within their expiry dates are included in this recall. The agency has classified this recall as Class II.

Consumers and healthcare providers should stop using the affected product and contact the manufacturer or their healthcare provider for further instructions.

The recalled product

Product
Magnesium Chloride Hexahydrate 82.5 mg/mL; Calcium Gluconate 30 mg/mL (PF), For IV Use, 10 mL Single Dose vial, Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321678355
Manufacturer
KRS Global Biotechnology, Inc
Category
Drug — IV Solution
Hazard
Affected units
878

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 remaining within expiry.

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 80 recalled by KRS Global Biotechnology, 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 80 products in this recall →

Related recalls

Same manufacturer · KRS Global Biotechnology, Inc

See all →

Same hazard · sterility

See all →

Similar recalls