Public recall detail

PENTAX Medical ultrasound endoscopes and water bottle assembly

2026-10-02

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Health products Health product recall
Quick summary

Quick summary: PENTAX Medical ultrasound endoscopes and water bottle assembly. Reason: Health product recall. Category: Health products. Date: 2026-10-02.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: PENTAX Medical ultrasound endoscopes and water bottle assembly. Reason: Health product recall. Category: Health products. Date: 2026-10-02.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandPentax Medical Corporation
ProductPENTAX Medical ultrasound endoscopes and water bottle assembly
IssueMedical devices - Labelling and packaging
Recall classType II
IdentificationRA-82698

Affected products

ProductWater Bottle Assembly
LotAll lots.
ModelOS-H5
Serial numberAll lots.
DescriptionWater Bottle Assembly
ProductUltrasound Endoscope
LotAll lots.
ModelEG34-J10U
Serial numberAll lots.
DescriptionUltrasound Endoscope
ProductUltrasound Endoscope
LotAll lots.
ModelEG38-J10UT
Serial numberAll lots.
DescriptionUltrasound Endoscope
ProductUltrasound Endoscope
LotAll lots.
ModelEG-3270UK
Serial numberAll lots.
DescriptionUltrasound Endoscope
ProductUltrasound Endoscope
LotAll lots.
ModelEG36-J10UR
Serial numberAll lots.
DescriptionUltrasound Endoscope
ProductUltrasound Endoscope
LotAll lots.
ModelEG-3670URK
Serial numberAll lots.
DescriptionUltrasound Endoscope
ProductUltrasound Endoscope
LotAll lots.
ModelEG-3870UTK
Serial numberAll lots.
DescriptionUltrasound Endoscope

Issue

Pentax Medical has received an information related to a reported patient death in connection with a case in which air unintentionally entered the balloon attached to the distal end of an ultrasound endoscope during an endoscopic ultrasonography procedure.As a result of the investigation, a definitive causal relationship between the ingress of air into the balloon and the patient's death could not be established. However, it also cannot be completely ruled out. Therefore, to clearly address this potential risk, Pentax Medical has added a new warning to the IFU for the relevant ultrasound endoscopes and the water bottle assembly. This additional warning will be included in the IFU of all newly manufactured devices. For devices already placed on the market the users shall add this field safety notice to their documentation and inform their staff accordingly.As this issue may, under certain circumstances, potentially lead to a serious adverse event, Pentax Medical provides the following information to all customers using ultrasound endoscopes to ensure continued safe use of our products.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use Health products - Medical devices - Gastroenterology and urology
CompaniesPentax Medical Corporation 1-1-110 Tsutsujigaoka, Tokyo, Tokyo-To, Japan, 196-0012
Recall date2026-09-14
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82698
Background{}
CompaniesPentax Medical Corporation 1-1-110 Tsutsujigaoka, Tokyo, Tokyo-To, Japan, 196-0012
AudiencesHealthcare
Source updated2026-10-02

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