Nico Corp. recalls NICO Shepherd's Hook (Part NN-8024) due to mislabeled pouch lacking critical product details like part numbers and expiration dates. Affected units sold with Lot 37LG1834 expiring Jan 2020.
Mislabeled hook pouch included a transport/storage label rather than the product label containing key product information such as part number, lot number, and expiration date, etc
Nico Corp. is recalling their Shepherd's Hook accessory for the BrainPath device because the included pouch has a transport label instead of the product label with important details like part numbers and expiration dates. This could lead to confusion about the product's status and safety.
The hook pouch includes a transport label instead of the product label, meaning it doesn't contain critical information like part numbers, lot numbers, or expiration dates. This could cause confusion about the product's status and safety, but it doesn't pose a direct physical hazard.
Users of the NICO Shepherd's Hook accessory (Part NN-8024) with Lot Number 37LG1834, which expired January 2020. Medical device users who rely on this accessory for BrainPath procedures are most at risk.
Check for the NICO Shepherd's Hook accessory with Part Number NN-8024 and Lot Number 37LG1834, which expired January 2020. The pouch should have the product label with part numbers and expiration dates.
Ensure the pouch has the product label with part number, lot number, and expiration date instead of a transport label.
The pouch includes a transport label instead of the product label with critical information like part numbers and expiration dates.
Check if the pouch has the product label with part number, lot number, and expiration date. If not, contact Nico Corp. for guidance.
No, this is a labeling issue that doesn't pose a direct physical hazard but could cause confusion about product status.
We’ve drafted a message you can send Nico Corp. to request your refund or repair — edit it as you like.
Subject: Recall Z-2822-2018 — Nico Corp. Nico Corp. Hello, I own a Nico Corp. that is covered by recall Z-2822-2018 from Nico Corp.. 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.
