The Recall Desk
ModerateFDA (Devices)·Z-1033-2019·Announced 2019-03-27

ACell Recalls Gentrix Surgical Matrix Thick Due to Tensile Strength Failure

ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick because a sample failed to meet tensile strength specifications.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, but the source text does not report any hospitalizations, injuries, or illnesses, fitting the criteria for a moderate severity score.

Plain-English summary

ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick, 20 x 30cm (Catalog Number PSMT2030, Lot 013948). This medical device is intended for implantation to reinforce soft tissue in patients requiring gastroenterological or plastic and reconstructive surgery, including hernia and body wall repair.

The recall was initiated because one sample from the affected lot failed to meet the company's tensile strength specification for lot release. The agency classified this recall as Class II.

The affected product was distributed nationwide in the state of California. Consumers and healthcare providers should stop using the recalled product and contact ACell, Inc. for further instructions.

The recalled product

Product
Gentrix Surgical Matrix Thick, 20 x 30cm, Catalog Number PSMT2030, Lot 013948 - Product Usage: Gentrix Surgical Matrix Thick is intended for implantation to reinforce soft tissue where weakness exists in patients requiring gastroenterological or plastic and reconstructive surgery
Manufacturer
ACell, Inc
Category
Medical Device — Surgical Implant
Hazard
Affected units
1

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • SN KJ000423

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 2 recalled by ACell, Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Related recalls

Same manufacturer · ACell, Inc

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Same hazard · structural failure

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