American Regent recalls Multrys (Trace Elements Injection 4, USP) vials due to hair, glass and paraformaldehyde contamination. Affected lots expire 4/30/2027. Contact for return instructions.
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
American Regent is recalling Multrys IV injection vials that may contain hair, glass, or paraformaldehyde particles. This contamination could cause serious injury if injected. The affected vials have specific lot numbers and expiration dates.
The product contains particulate matter including hair, glass, and paraformaldehyde. When injected intravenously, these particles could cause blockages, infections, or severe reactions in the bloodstream.
Healthcare professionals using the recalled Multrys vials for intravenous infusion. Patients receiving the injection could be at risk if the contaminated product is administered.
Check for vials labeled 'Multrys (Trace Elements Injection 4, USP)' with NDC 0517-9302-01 (1 mL single-dose) or NDC 0517-9302-25 (25x1 mL). The affected lot number is 25163, expiring 4/30/2027.
Immediately stop using the recalled Multrys vials if you have them. Do not administer the product to patients.
The product contains particulate matter including hair, glass, and paraformaldehyde.
Vials with NDC 0517-9302-01 (1 mL single-dose) or NDC 0517-9302-25 (25x1 mL) lot 25163, expiring 4/30/2027.
Look for vials labeled 'Multrys (Trace Elements Injection 4, USP)' with the specific NDC numbers and lot 25163.
We’ve drafted a message you can send American Regent to request your refund or repair — edit it as you like.
Subject: Recall D-0799-2026 — American Regent American Regent Hello, I own a American Regent that is covered by recall D-0799-2026 from American Regent. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
