Surepulse recalls VS Cap Large (REF: SP-162-A1) for newborn heart rate monitor due to incorrect sizing guide in labeling. Consumers should check their product details.
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
Surepulse is recalling a specific cap component for newborn heart rate monitors because the labeling has an incorrect sizing guide. This could lead to improper fitting if the cap is not sized correctly for the baby's head.
The cap's labeling has an incorrect sizing guide, which might cause it to be too large or too small for the baby's head. This could lead to improper monitoring of the baby's heart rate.
New parents using the Surepulse VS Newborn Heart Rate Monitor with the specific cap model (REF: SP-162-A1) are most at risk if the cap doesn't fit properly.
Check if your Surepulse VS Newborn Heart Rate Monitor includes the cap with reference number SP-162-A1. The cap was sold with specific production lots from 13816 to 13840.
Look for the cap reference number SP-162-A1 on your Surepulse VS Newborn Heart Rate Monitor.
The recall is for incorrect labeling, not a safety hazard. The cap itself is safe but may not fit properly if the sizing guide is wrong.
No, you can continue using the monitor as long as you check the cap's sizing guide and ensure it fits properly.
The recall does not provide a remedy, so contact Surepulse directly for guidance on proper sizing.
We’ve drafted a message you can send Surepulse to request your refund or repair — edit it as you like.
Subject: Recall Z-1359-2026 — Surepulse Surepulse Hello, I own a Surepulse that is covered by recall Z-1359-2026 from Surepulse. 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.