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Lower risk Medical device recall · FDA · Published June 21, 2018

Johnson & Johnson Surgical Vision Recalls Expired Intraocular Lenses

Johnson & Johnson Surgical Vision recalls expired Abbott TECNIS 1-Piece Aspheric Acrylic IOLs with TECNIS iTEC Preloaded Delivery System. Lenses manufactured before their expiration dates may cause vision issues.

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Recalling firmJohnson & Johnson Surgical Vision Inc1700 E Saint Andrew Pl · Santa Ana, CA 92705-4933
✎ GovInfoNow plain-language explainer

What happened, in plain English

Johnson & Johnson Surgical Vision has recalled expired Abbott TECNIS intraocular lenses. Using these expired lenses could lead to vision problems since they were distributed past their expiration dates. Read more at govinfonow.com/recall/70812-johnson-johnson-surgical-vision-recalls-expired-intraocular-lenses.

Source Summary by GovInfoNow · govinfonow.com/recall/70812-johnson-johnson-surgical-vision-recalls-expired-intraocular-lenses · Updated August 20, 2026 · FDA enforcement record: FDA #Z-0464-2019

Cite this page

“Johnson & Johnson Surgical Vision Recalls Expired Intraocular Lenses.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/70812-johnson-johnson-surgical-vision-recalls-expired-intraocular-lenses. Based on FDA recall #Z-0464-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0464-2019%22&limit=1).

Why it’s dangerous

The lenses were distributed after their expiration dates. Expired intraocular lenses may not function properly and could lead to vision problems if used in surgery.

Who’s affected

Patients who received these specific intraocular lenses for cataract surgery are affected. Those with expired lenses may experience vision issues but are unlikely to face serious harm.

How to tell if you have this one

Check for the lens model PCB00 and expiration dates listed on the packaging (e.g., 3/11/2018, 10/9/2017). The product includes specific serial numbers and expiration dates for each item.

  • Brand
    Johnson & Johnson Surgical Vision
  • Product
    Johnson & Johnson Surgical Vision Inc recalls Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Preloaded Delivery System, Lens Model PCB00,…
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Expiration Date

    Look for the expiration date on the lens packaging or product label to confirm if it's expired.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 7 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: named in the noticeWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: named in the noticeMNIllinois: nationwideILWisconsin: nationwideWIMichigan: nationwideMINew York: nationwideNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: named in the noticeNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: named in the noticeINOhio: nationwideOHPennsylvania: nationwidePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: nationwideCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: named in the noticeWVVirginia: nationwideVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: nationwideTNNorth Carolina: named in the noticeNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: nationwideGAHawaii: nationwideHITexas: named in the noticeTXFlorida: nationwideFL

FDA distribution: “US Nationwide distribution in the states of IN, MN, NC, NV, TX, and WA, WV. There was no foreign/military/government distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Indiana, Minnesota, Nevada, North Carolina, Texas, Washington, West Virginia.

Recall timeline

FDA terminated this recall 2.9 years after the firm started it.

1. Firm started the recall: Jun 21, 201812. FDA classified it Class II: Nov 14, 201823. Published in FDA’s Enforcement Report: Nov 21, 201834. FDA terminated the recall: Apr 28, 2021420182021
  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

Do I need to do anything if my lenses are expired?

Yes, you should check the expiration date and contact your eye doctor to discuss potential vision issues.

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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-0464-2019 (June 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0464-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on August 20, 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