CLASS II ONGOING Device recall · Reported 17 Apr 2024 · FDA Enforcement Report

Acetabular Bearing (xx)MM I.D X (xx) O.D recalled by Synovo Production

Synovo Production is recalling Acetabular Bearing (xx)MM I.D X (xx) O.D. Uhmwpe 1020, Sterileeo, Reference Numbers, distributed nationwide in the US. The recall was initiated on 30 May 2023 and the FDA has classified it as Class II.

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Lot, batch or date codesUDI/REF Number: 00814193025906/01-02-4254; 00814193025913/01-02-4456; 00814193025920/01-02-4558; 00814193025937/01-02-4760; 00814193025968/01-02-4962; 00814193025944/01-02-5164; 00814193025951/01-02-5266; REF Number/Lot Number: 01-02-4254 01024254FNN612, 01-02-4254 01024254FNN613, 01-02-4254 01024254GNN614, 01-02-4254 01024254FNN620, 01-02-4254 01024254GNN623, 01-02-4254 01024254FNN644, 01-02-4254 01024254NN651, 01-02-4254 01024254NN652, 01-02-4254 01024254NN741, 01-02-4456 01024456ENN613, 01-02-4456 01024456FNN614, 01-02-4456 01024456ENN620, 01-02-4456 01024456FNN620, 01-02-4456 01024456FNN623, 01-02-4456 01024456ENN644, 01-02-4456 01024456FNN644, 01-02-4456 01024456ENN650, 01-02-4456 01024456FNN650, 01-02-4456 01024456NN651, 01-02-4456 01024456NN652, 01-02-4456 01024456NN656, 01-02-4456 01024456NN728, 01-02-4458 01024458NN651, 01-02-4458 01024458NN652, 01-02-4558 01024558FNN614, 01-02-4558 01024558FNN623, 01-02-4558 01024558NN629, 01-02-4558 01024558HNN686, 01-02-4558 01024558HNN692, 01-02-4558 01024558JNN698, 01-02-4760 01024760FNN614, 01-02-4760 01024760ENN616, 01-02-4760 01024760ENN620, 01-02-4760 01024760FNN620, 01-02-4760 01024760FNN623, 01-02-4760 01024760ENN625, 01-02-4760 01024760FNN644, 01-02-4760 01024760NN651, 01-02-4760 01024760NN652, 01-02-4760 01024760NN654, 01-02-4760 01024760NN656, 01-02-4760 01024760HNN698, 01-02-4760 01024760HNN728, 01-02-4760 01024760HNN741, 01-02-4962 01024962FNN614, 01-02-4962 01024962ENN616, 01-02-4962 01024962FNN622, 01-02-4962 01024962NN624, 01-02-4962 01024962NN628, 01-02-4962 01024962NN645, 01-02-4962 01024962ENN654, 01-02-4962 01024962NN668, 01-02-4962 01024962NN670, 01-02-4962 01024962HNN686, 01-02-4962 01024962HNN723, 01-02-4962 01024962NN734, 01-02-4962 01024962NN735, 01-02-5164 01025164ENN614, 01-02-5164 01025164ENN620, 01-02-5164 01025164ENN622, 01-02-5164 01025164NN634, 01-02-5164 01025164NN649, 01-02-5164 01025164NN656, 01-02-5164 01025164NN669, 01-02-5164 01025164GNN678, 01-02-5164 01025164GNN680, 01-02-5164 01025164GNN691, 01-02-5164 01025164HNN695, 01-02-5164 01025164HNN697, 01-02-5164 01025164JNN733, 01-02-5164 01025164JNN743, 01-02-5266 01025266NN639, 01-02-5266 01025266NN654, 01-02-5266 01025266NN656, 01-02-5266 01025266CNN664, 01-02-5266 01025266CNN670, 01-02-5266 01025266CNN691, 01-02-5266 01025255CNN692, 01-02-5266 01025266DNN698, 01-02-5266 01025266ENN733,

Quantity recalled1681 units

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-1497-2024
FDA event ID: 94278
Recalling firm: Synovo Production, Fullerton, CA
Classification: Class II
Status: Ongoing
Recall initiated: 30 May 2023
FDA classified: 8 Apr 2024
Reported: 17 Apr 2024
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Other Reasons
Device type: Hip & Knee Implants

Timeline

30 May 2023	Recall initiated by company
8 Apr 2024	Classified by FDA	+314 days
17 Apr 2024	Published in enforcement report	+9 days

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

Reason for recall

Medical device components were marketed without FDA clearance

Product as listed by the FDA

ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020, STERILEEO, Reference Numbers: 01-02-4254 01-02-4456 01-02-4558 01-02-4760 01-02-4962 01-02-5164 01-02-5266

Where it was distributed

US Nationwide distribution in the state of WA.

Nationwide Washington

Questions about this recall

Why was it recalled?

Medical device components were marketed without FDA clearance

Which lots are affected?

UDI/REF Number: 00814193025906/01-02-4254; 00814193025913/01-02-4456; 00814193025920/01-02-4558; 00814193025937/01-02-4760; 00814193025968/01-02-4962; 00814193025944/01-02-5164; 00814193025951/01-02-5266; REF Number/Lot Number: 01-02-4254 01024254FNN612, 01-02-4254 01024254FNN613, 01-02-4254 01024254GNN614, 01-02-4254 01024254FNN620, 01-02-4254 01024254GNN623, 01-02-4254 01024254FNN644, 01-02-4254 01024254NN651, 01-02-4254 01024254NN652, 01-02-4254 01024254NN741, 01-02-4456 01024456ENN613, 01-02-4456 01024456FNN614, 01-02-4456 01024456ENN620, 01-02-4456 01024456FNN620, 01-02-4456 01024456FNN623, 01-02-4456 01024456ENN644, 01-02-4456 01024456FNN644, 01-02-4456 01024456ENN650, 01-02-4456 01024456FNN650, 01-02-4456 01024456NN651, 01-02-4456 01024456NN652, 01-02-4456 01024456NN656, 01-02-4456 01024456NN728, 01-02-4458 01024458NN651, 01-02-4458 01024458NN652, 01-02-4558 01024558FNN614, 01-02-4558 01024558FNN623, 01-02-4558 01024558NN629, 01-02-4558 01024558HNN686, 01-02-4558 01024558HNN692, 01-02-4558 01024558JNN698, 01-02-4760 01024760FNN614, 01-02-4760 01024760ENN616, 01-02-4760 01024760ENN620, 01-02-4760 01024760FNN620, 01-02-4760 01024760FNN623, 01-02-4760 01024760ENN625, 01-02-4760 01024760FNN644, 01-02-4760 01024760NN651, 01-02-4760 01024760NN652, 01-02-4760 01024760NN654, 01-02-4760 01024760NN656, 01-02-4760 01024760HNN698, 01-02-4760 01024760HNN728, 01-02-4760 01024760HNN741, 01-02-4962 01024962FNN614, 01-02-4962 01024962ENN616, 01-02-4962 01024962FNN622, 01-02-4962 01024962NN624, 01-02-4962 01024962NN628, 01-02-4962 01024962NN645, 01-02-4962 01024962ENN654, 01-02-4962 01024962NN668, 01-02-4962 01024962NN670, 01-02-4962 01024962HNN686, 01-02-4962 01024962HNN723, 01-02-4962 01024962NN734, 01-02-4962 01024962NN735, 01-02-5164 01025164ENN614, 01-02-5164 01025164ENN620, 01-02-5164 01025164ENN622, 01-02-5164 01025164NN634, 01-02-5164 01025164NN649, 01-02-5164 01025164NN656, 01-02-5164 01025164NN669, 01-02-5164 01025164GNN678, 01-02-5164 01025164GNN680, 01-02-5164 01025164GNN691, 01-02-5164 01025164HNN695, 01-02-5164 01025164HNN697, 01-02-5164 01025164JNN733, 01-02-5164 01025164JNN743, 01-02-5266 01025266NN639, 01-02-5266 01025266NN654, 01-02-5266 01025266NN656, 01-02-5266 01025266CNN664, 01-02-5266 01025266CNN670, 01-02-5266 01025266CNN691, 01-02-5266 01025255CNN692, 01-02-5266 01025266DNN698, 01-02-5266 01025266ENN733,

Where was it sold?

US Nationwide distribution in the state of WA.

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

Other products in this recall event

2 other products · FDA event 94278

This product is part of a recall event; the main page for the event is Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V Eli recalled.

Reported	Class	Recall	Company	Reason	Where
17 Apr 2024	CLASS II	Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V Eli recalled	Synovo Production	Other	Nationwide
17 Apr 2024	CLASS II	Acetabular Fixation Cup, (xx)MM, 5 Hole recalled by Synovo Production	Synovo Production	Other	Nationwide

More recalls from Synovo Production

All 3

Reported	Class	Recall	Company	Reason	Where
17 Apr 2024Device	CLASS II	Acetabular Fixation Cup, (xx)MM, 5 Hole recalled by Synovo Production	Synovo Production	Other	Nationwide
17 Apr 2024Device	CLASS II	Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V Eli recalled	Synovo Production	Other	Nationwide

Other Hip & Knee Implants recalls

All 3,097

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12 Aug 2026Device	CLASS II	U2 Total Knee System Femoral offset bushing recalled	United Orthopedic	Device Malfunction	Nationwide