CLASS II Device recall · Reported 29 Mar 2017 · FDA Enforcement Report

MotoCLIP(TM) Super Elastic Fusion System, Size recalled

Crossroads Extremity Systems is recalling MotoCLIP(TM) Super Elastic Fusion System, Size, distributed in 7 states. The recall was initiated on 16 Feb 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Number 101868

Quantity recalled20 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-1487-2017
FDA event ID: 76687
Recalling firm: Crossroads Extremity Systems, Memphis, TN
Classification: Class II
Status: Terminated
Recall initiated: 16 Feb 2017
FDA classified: 20 Mar 2017
Reported: 29 Mar 2017
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

16 Feb 2017	Recall initiated by company
20 Mar 2017	Classified by FDA	+32 days
29 Mar 2017	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

Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.

Product as listed by the FDA

MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.

Where it was distributed

Al, FL, IN, Il, NE, TX, NM, CO, AZ

Arizona Colorado Florida Indiana Nebraska New Mexico Texas

Questions about this recall

Why was it recalled?

Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.

Which lots are affected?

Lot Number 101868

Where was it sold?

Al, FL, IN, Il, NE, TX, NM, CO, AZ

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.

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