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Lower risk Medical device recall · FDA · Published August 10, 2017

Synthes Norian Drillable Inject: Kit expiration dates may be outdated

Synthes recalls Norian Drillable Inject kits with potential expiration date mismatches. Some components expire before the kit's listed expiration date, which could lead to improper use. Affected kits have product number 07.704.010S and lot number DSE0733.

🇺🇸 FDA recall #Z-0618-2018Medical deviceSynthes ›
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Recalling firmSynthes USA1230 Wilson Dr · West Chester, PA 19380-4231
✎ GovInfoNow plain-language explainer

What happened, in plain English

Synthes is recalling Norian Drillable Inject kits because some components expire before the kit's listed expiration date. This mismatch could lead to using expired components, potentially causing improper use of the product. Read more at govinfonow.com/recall/73149-synthes-norian-drillable-inject-kit-expiration-dates-may-be-outdated.

Source Summary by GovInfoNow · govinfonow.com/recall/73149-synthes-norian-drillable-inject-kit-expiration-dates-may-be-outdated · Updated September 18, 2026 · FDA enforcement record: FDA #Z-0618-2018

Cite this page

“Synthes Norian Drillable Inject: Kit expiration dates may be outdated.” GovInfoNow, updated September 18, 2026. https://govinfonow.com/recall/73149-synthes-norian-drillable-inject-kit-expiration-dates-may-be-outdated. Based on FDA recall #Z-0618-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0618-2018%22&limit=1).

Why it’s dangerous

The kit's expiration date may be later than the earliest expiration date of the components inside it. This means some components could expire before the kit's listed expiration date, leading to potential use of expired materials.

Who’s affected

Users of Norian Drillable Inject kits with product number 07.704.010S and lot number DSE0733 are affected. The risk is low as this is a potential expiration mismatch rather than a safety hazard.

How to tell if you have this one

Check for product number 07.704.010S and lot number DSE0733 on the kit. This specific kit has a potential expiration date mismatch.

  • Brand
    Synthes
  • Category
    Medical device
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide Distribution.
Recall numberProduct, codes & lotsQuantity
Z-0617-2018Norian Drillable Inject; Product Number: 07.704.003S Lot Number: DSD9110239 units
Z-0618-2018Norian Drillable Inject; Product Number: 07.704.010S Lot Number: DSE07335 units
Based on the official FDA remedy

What to do — step by step

  1. Check Kit Expiration Dates

    Verify the kit's expiration date against the earliest expiration date of its components.

Where it went and when

Where it was distributed

Distributed nationwide.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 13 months after the firm started it.

1. Firm started the recall: Aug 10, 201712. FDA classified it Class II: Feb 15, 201823. Published in FDA’s Enforcement Report: Feb 21, 201834. FDA terminated the recall: Sep 10, 2018420172018
  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.

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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-0618-2018 (August 10, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0618-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on September 18, 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