The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-1088-2020·Announced 2020-02-12

Centurion OR2020 Basin Set Recalled for Incomplete Sterile Seals

Centurion Medical Products is recalling 188 units of the OR2020 Basin Set because incomplete seals may compromise sterility.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a risk-of-harm product (compromised sterility) where injury has not yet been reported, fitting the High severity criteria.

Plain-English summary

Centurion Medical Products Corporation is recalling 188 units of the OR2020 Basin Set. The recall is due to incomplete seals on the sterile package, which may compromise the sterility of the product.

The affected units are identified by lot codes 2019020790 and 2018111990. The product was distributed nationwide and to Ghana.

Consumers and healthcare facilities should stop using the affected basin sets and contact Centurion Medical Products Corporation for further instructions.

The recalled product

Product
Centurion- OR2020 BASIN SET
Affected units
188

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 (2)

  • Lot Codes: 2019020790
  • 2018111990

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 54 recalled by Centurion Medical Products Corporation 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 54 products in this recall →

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