CLASS II Device recall · Reported 13 Nov 2019 · FDA Enforcement Report

Cable-ready Short Gtr and Cable-ready Long Gtr recalled by Zimmer Biomet

Zimmer Biomet is recalling Cable-ready Short Gtr and Cable-ready Long Gtr, distributed nationwide in the US. The recall was initiated on 10 Oct 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes77001932 77001933 77001878 62176030 62112090 62146839

Quantity recalled5,459,583 total devices

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0327-2020
FDA event ID: 83962
Recalling firm: Zimmer Biomet, Warsaw, IN
Classification: Class II
Status: Terminated
Recall initiated: 10 Oct 2019
FDA classified: 7 Nov 2019
Reported: 13 Nov 2019
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Packaging Defects
Device type: Other Medical Devices

Timeline

10 Oct 2019	Recall initiated by company
7 Nov 2019	Classified by FDA	+28 days
13 Nov 2019	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202

Where it was distributed

Distributed nationwide.

Nationwide

Questions about this recall

Is Cable-ready Short Gtr and Cable-ready Long Gtr recalled?

Yes. Zimmer Biomet recalled Cable-ready Short Gtr and Cable-ready Long Gtr on 10 Oct 2019. The recall is Class II and its status is Terminated. Recall number Z-0327-2020.

Why was it recalled?

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Which lots are affected?

77001932 77001933 77001878 62176030 62112090 62146839

Where was it sold?

Distributed nationwide.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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