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Lower risk Medical device recall · FDA · Published December 13, 2017

Signia" Power Handle

C17AAG

🇺🇸 FDA recall #Z-1237-2018Medical deviceC17AAG ›
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Contact the company

Recalling firmCovidien LLC60 Middletown Ave · North Haven, CT 06473-3908
✎ GovInfoNow plain-language explainer

What happened, in plain English

Source Summary by GovInfoNow · govinfonow.com/recall/72330-c17aag · Updated August 31, 2026 · FDA enforcement record: FDA #Z-1237-2018

Cite this page

“Signia" Power Handle.” GovInfoNow, updated August 31, 2026. https://govinfonow.com/recall/72330-c17aag. Based on FDA recall #Z-1237-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1237-2018%22&limit=1).

Why it’s dangerous

low_risk

Who’s affected

all

How to tell if you have this one

C17AAG

  • Brand
    C17AAG
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. 1

    Check the product name and manufacturer for any signs of tampering or unauthorized changes.

  2. 2

    Ensure that the product is from a reputable manufacturer and has a valid certification.

  3. 3

    Contact the manufacturer or a healthcare professional if you have concerns about the product.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide Distribution: US (Nationwide).” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 2.3 years after the firm started it.

1. Firm started the recall: Dec 13, 201712. FDA classified it Class II: Mar 27, 201823. Published in FDA’s Enforcement Report: Apr 4, 201834. FDA terminated the recall: Apr 14, 2020420172020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What is C17AAG?

C17AAG is a product code used by Covidien LLC for medical devices.

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Where this comes from

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.

  • Official source: FDA Recall #Z-1237-2018 (December 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1237-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on August 31, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA