FDAClass IIJuly 17, 2024

BPKN15C KNEE BASIN PACK BHS- Procedure tray recall

BPKN15C KNEE BASIN PACK BHS- Procedure tray Catalog Number: BPKN15C

Why was BPKN15C KNEE BASIN PACK BHS- Procedure tray recalled?

Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: 00191072200518 LOT#"s: 639231 928241

Product
BPKN15C KNEE BASIN PACK BHS- Procedure tray Catalog Number: BPKN15C
Recalling firm
American Contract Systems Inc
Quantity
552 units
Distribution
US Nationwide distribution.
Recall date
July 17, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls