Pajunk recalls continuous epidural trays with incorrect 2ml Marcaine Spinal ampule instead of 10ml Sodium Chloride. This could cause unsafe anesthesia levels during procedures.
The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml ampule of 0.9% Sodium Chloride as intended,.
Pajunk is recalling continuous epidural trays that contain a 2ml ampule of 0.75% Marcaine Spinal instead of the intended 10ml ampule of 0.9% Sodium Chloride. This error could lead to unsafe anesthesia levels during medical procedures.
The tray contains a 2ml ampule of 0.75% Marcaine Spinal instead of the required 10ml ampule of 0.9% Sodium Chloride. This incorrect medication concentration could lead to unsafe anesthesia levels during procedures, potentially causing adverse effects in patients.
Healthcare professionals using Pajunk continuous epidural trays for spinal anesthesia procedures. Patients receiving epidural anesthesia from these trays are at risk of incorrect medication dosing.
Check for the model #TAL101 on the tray. The product was sold with lot number 0001359, expiring April 2024. The UDI code starts with 01 00858965006007(17)240401(10)0001859.
Verify the model number and lot information on the tray to confirm if it is affected.
The tray contains a 2ml ampule of 0.75% Marcaine Spinal instead of the intended 10ml ampule of 0.9% Sodium Chloride.
The recall record does not specify a remedy, so check the product details to confirm if it is affected.
Look for model #TAL101, lot number 0001359, and the UDI code starting with 01 00858965006007(17)240401(10)0001859.
We’ve drafted a message you can send Pajunk to request your refund or repair — edit it as you like.
Subject: Recall Z-0278-2023 — Pajunk Pajunk Hello, I own a Pajunk that is covered by recall Z-0278-2023 from Pajunk. 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.
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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.
