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Viona Pharmaceuticals Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count HDPE bottles NDC# 72578-036-01 - safety alert

Official notice

2 Feb 2022

Last checked

2 Feb 2022

Medium riskFDA

An official FDA notice concerns Viona Pharmaceuticals Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count HDPE bottles NDC# 72578-036-01 - safety alert. An official FDA notice concerns Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count HDPE bottles NDC# 72578-036-01. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2022-02-02. Recall numbers: D-0392-2022. Check the official notice for the complete list. Published 2022-02-02.

What to do now

The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.

Units affected

238,416

Recall number

D-0392-2022

Official notice

2022-02-02

The hazard

An official FDA notice concerns Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count HDPE bottles NDC# 72578-036-01. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2022-02-02. Recall numbers: D-0392-2022. Check the official notice for the complete list.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Event Ids

89305

Recall Numbers

D-0392-2022

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Affected products

Product 1

Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count HDPE bottles NDC# 72578-036-01

Units affected

238,416

Risk / hazard

An official FDA notice concerns Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count HDPE bottles NDC# 72578-036-01. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2022-02-02. Recall numbers: D-0392-2022. Check the official notice for the complete list.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · NJ · Cranford

Affected area 1

US · United States · NJ · Cranford

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Viona Pharmaceuticals. Contact: VIONA PHARMACEUTICALS INC.

Source & status

Source

Tier

official

Category

HEALTH

App estimate

medium

Recall details

Recall number

D-0392-2022

Event id

89305

Units affected

238,416

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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