CLASS II Device recall · Reported 30 Dec 2020 · FDA Enforcement Report

IceSeed" 5 Cryoablation Needle recalled by Boston Scientific

Boston Scientific is recalling IceSeed" 5 Cryoablation Needle, distributed nationwide in the US. The recall was initiated on 18 Nov 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUPN: FPRPR3201 UDIs: 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181 Batch Numbers: U0181, T0393, A6912, A6664, A1915, A1072, A1024, A0853, A0574
Quantity recalled152 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-0676-2021
FDA event ID
86777
Recalling firm
Boston Scientific, Maple Grove, MN
Classification
Class II
Status
Completed
Recall initiated
18 Nov 2020
FDA classified
22 Dec 2020
Reported
30 Dec 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects

Timeline

18 Nov 2020Recall initiated by company
22 Dec 2020Classified by FDA+34 days
30 Dec 2020Published in enforcement report+8 days

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

Reason for recall

Complaint trend regarding needle shaft gas leaks.

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

IceSeed" 1.5 Cryoablation Needle

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is IceSeed" 5 Cryoablation Needle recalled?

Yes. Boston Scientific recalled IceSeed" 5 Cryoablation Needle on 18 Nov 2020. The recall is Class II and its status is Completed. Recall number Z-0676-2021.

Why was it recalled?

Complaint trend regarding needle shaft gas leaks.

Which lots are affected?

UPN: FPRPR3201 UDIs: 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181, 7290104830181 Batch Numbers: U0181, T0393, A6912, A6664, A1915, A1072, A1024, A0853, A0574

Where was it sold?

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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