CLASS II Device recall · Reported 26 Feb 2020 · FDA Enforcement Report

1 Stratafix" Spiral PDS Plus Violet 12" CT-1 Needle, SXPP1B429 recalled

Ethicon is recalling 1 Stratafix" Spiral PDS Plus Violet 12" CT-1 Needle, SXPP1B429. The recall was initiated on 28 Aug 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesGTIN: 10705031235816 Lot Number: PAH166 Expiration Date: 12/31/2020
Quantity recalled133 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-1336-2020
FDA event ID
84772
Recalling firm
Ethicon, Somerville, NJ
Classification
Class II
Status
Terminated
Recall initiated
28 Aug 2019
FDA classified
20 Feb 2020
Reported
26 Feb 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

28 Aug 2019Recall initiated by company
20 Feb 2020Classified by FDA+176 days
26 Feb 2020Published 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

The product do not meet certain internal testing specifications.

Product as listed by the FDA

1 STRATAFIX" Spiral PDS Plus Violet 12" (30 cm) CT-1 Needle, SXPP1B429

Where it was distributed

International: Australia, Hong King, India, Japan, Korea, Singapore, Thailand

Questions about this recall

Why was it recalled?

The product do not meet certain internal testing specifications.

Which lots are affected?

GTIN: 10705031235816 Lot Number: PAH166 Expiration Date: 12/31/2020

Where was it sold?

International: Australia, Hong King, India, Japan, Korea, Singapore, Thailand

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 84772

This product is part of a recall event; the main page for the event is 1 Stratafix Spiral PDS Plus Violet 18" OS-6 Needle, SXPP1B201 recalled.

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