HIGHFDA DRUG

Magnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk active pharmaceutical ingredient (API), Avantor Performance Materials, LLC, 100 Matsonford Road, Suite 200, Radnor, PA 19087, NDC...

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
March 31, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
March 31, 2026
Hazard Level
HIGH
Brand
Avantor Performance Materials
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Avantor Performance Materials
Model numbers
Lot 23G3161005, Exp 9/21/2027
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    March 31, 2026

  2. Reported by FDA DRUG

    April 22, 2026

  3. RecallRadar source check

    April 29, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Subpotent drug

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Avantor Performance Materials LLC or your healthcare provider for guidance. Notification method: Letter

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Full Description

Magnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk active pharmaceutical ingredient (API), Avantor Performance Materials, LLC, 100 Matsonford Road, Suite 200, Radnor, PA 19087, NDC 10106-2448-1. Reason: Subpotent drug. Classification: Class III. Quantity: 36 bottles. Distribution: Nationwide in the USA, Belgium and France

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Lot 23G3161005
Exp 9/21/2027
Affected States
ALL
Report Date
April 22, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE