Windstone Medical Packaging recalls AMS ALIGNED MEDICAL SOLUTIONS SPINAL KIT kits with specific part numbers due to supplier quality issues with Lidocaine HCl injection.
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier quality issues.
Windstone Medical Packaging is recalling specific SPINAL KIT medical convenience kits that contain Elevaris Lidocaine HCl injection USP. The recall is due to supplier quality issues with the lidocaine product, which could pose a safety risk.
The recall is due to supplier quality issues with Elevar: Lidocaine HCl injection USP. This means the lidocaine product may not meet quality standards, potentially affecting safety during medical procedures.
Healthcare professionals and medical facilities that use these SPINAL KIT kits are likely affected. Those handling the specific part numbers are at the highest risk.
Check for SPINAL KIT kits with part number AMS13683A and lot number 230451. These kits are labeled with UDI/DI B098AMS13683A0.
Verify the part number and lot number on the kit to confirm if it is recalled.
The recall is due to supplier quality issues with Elevaris Lidocaine HCl injection USP.
The official notice does not specify a remedy or action steps for affected users.
The recall is for supplier quality issues, but the official notice does not describe a specific hazard mechanism that could cause serious injury.
We’ve drafted a message you can send Windstone Medical Packaging to request your refund or repair — edit it as you like.
Subject: Recall Z-2812-2026 — Windstone Medical Packaging Windstone Medical Packaging Hello, I own a Windstone Medical Packaging that is covered by recall Z-2812-2026 from Windstone Medical Packaging. 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.
