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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93222

22 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
September 25, 2023
Product types
Device
Classifications
Class II and Class III
Statuses
Ongoing
Recalling firm wording
Aizu Olympus Co., Ltd.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

22 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 22

Bronchoscope-for endoscopy and endoscopic surgery within the airways and tracheobronchial tree. Model Numbers: BF-1T150, BF-1T60, BF-1TH190, BF-1TQ170, BF-3C160, BF-3C40, BF-H190, BF-MP190F, BF-MP60, BF-P150, BF-P190, BF-P60, BF-Q170, BF-Q190, BF-XP190, BF-XP60, BF-XT160, BF-XT190. 510(k)s: K023984, K121959, K963033, K172726, K201758, K033225, K183419.

Z-0327-2024
Recall number
Z-0327-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
1123 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): BF-1T150 (04953170308185), BF-1T60 (04953170308161), BF-1TH190 (04953170335181), BF-1TQ170 (04953170342943), BF-3C160 (04953170340031), BF-3C40 (04953170308130), BF-H190 (04953170335174), BF-MP190F (04953170395581), BF-MP60 (04953170308277), BF-P150 (04953170308178), BF-P190 (04953170342110), BF-P60 (04953170308123), BF-Q170 (04953170342912), BF-Q190 (04953170335198), BF-XP190 (04953170342134), BF-XP60 (04953170308154), BF-XT160 (04953170340147), BF-XT190 (04953170402470).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 2 of 22

Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging, ultrasound guided needle aspiration and other endoscopic procedures within the airways, trancheobronchial tree, esophagus and surrounding organs Model Numbers: BF-UC180F, BF-UC190F.

Z-0328-2024
Recall number
Z-0328-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
823 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): BF-UC180F (04953170356360), BF-UC190F (04953170399831).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 3 of 22

Colonoscope: for endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum, sigmoid colon, colon and ileocecal valve). Model Numbers: CF-2T160I, CF-2T160L, CF-H170I, CF-H170L, CF-H180AI, CF-H180AL, CF-H180DI, CF-H180DL, CF-H190I, CF-H190L, CF-HQ190I, CF-HQ190L, CF-LV1I, CF-LV1L, CF-Q150I, CF-Q150L, CF-Q160S, CF-Q180AI, CF-Q180AL. 510(k) Numbers: K954451, K112680, K100584, K051645, K111756, K001241, K911278.

Z-0329-2024
Recall number
Z-0329-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
3344 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): CF-2T160I (04953170307645), CF-2T160L (04953170307652), CF-H170I (04953170334184), CF-H170L (04953170334160), CF-H180AI (04953170339585), CF-H180AL (04953170339608), CF-H180DI (04953170339639), CF-H180DL (04953170339653), CF-H190I (04953170305177), CF-H190L (04953170305153), CF-HQ190I (04953170305139), CF-HQ190L (04953170305115), CF-LV1I (04953170312410), CF-LV1L (04953170312397), CF-Q150I (04953170307621), CF-Q150L (04953170307638), CF-Q160S (04953170307669), CF-Q180AI (04953170307690), CF-Q180AL (04953170307706).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 4 of 22

Choleodochoscope. Model Numbers: CHF-BP30, CHF-CB30L, CHF-P60.

Z-0330-2024
Recall number
Z-0330-2024
Initiated
September 25, 2023
Classification
Class III
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
3 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): CHF-BP30 (04953170068751), CHF-CB30L (04953170340154), CHF-P60 (Not recorded).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 5 of 22

Cystonephroscope-endoscopic diagnosis and treatment within the bladder, urethra, and kidney Model Numbers: CYF-5, CYF-VH, CYF-VHR.

Z-0331-2024
Recall number
Z-0331-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
1243 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): CYF-5 (04953170292323), CYF-VH (04953170411250), CYF-VHR (04953170411298).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 6 of 22

Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal lumens and airway anatomy (including nasopharyngeal and trachea). Model Numbers: ENF-T3, ENF-VT2, ENF-VT3.

Z-0332-2024
Recall number
Z-0332-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
46 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): ENF-T3 (04953170307188), ENF-VT2 (04953170339509), ENF-VT3 (04953170411526).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 7 of 22

Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA) and for endoscopic surgery within the upper digestive tract. Model Numbers: GF-UC140P-AL5, GF-UCT180, GF-UE160-AL5.

Z-0333-2024
Recall number
Z-0333-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
680 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Numbers: GF-UC140P-AL5 (04953170356322), GF-UCT180 (04953170356339), GF-UE160-AL5 (04953170356261).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 8 of 22

Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model Numbers: GIF-1TH190, GIF-1TQ160, GIF-2T160, GIF-2TH180, GIF-H170, GIF-H180, GIF-H180J, GIF-H190, GIF-HQ190, GIF-LV1, GIF-N180, GIF-Q150, GIF-Q160Z, GIF-Q180, GIF-XP180N, GIF-XP190N, GIF-XTQ160. 510(k) Numbers: K112680, K954451, K051645, K100584, K111756, K011151, K123317.

Z-0334-2024
Recall number
Z-0334-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
3627 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Numbers: GIF-1TH190 (04953170343360), GIF-1TQ160 (Not recorded), GIF-2T160 (04953170307492), GIF-2TH180 (04953170339745), GIF-H170 (04953170334115), GIF-H180 (04953170339769), GIF-H180J (04953170307539), GIF-H190 (04953170305290), GIF-HQ190 (04953170305276), GIF-LV1 (04953170312373), GIF-N180 (04953170307508), GIF-Q150 (04953170307485), GIF-Q160Z (04953170066795), GIF-Q180 (04953170307522), GIF-XP180N (04953170307515), GIF-XP190N (04953170305313), GIF-XTQ160 (04953170339837).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 9 of 22

Hysteroscope-For endoscopic diagnosis within the uterus Model Number: HYF-1T.

Z-0335-2024
Recall number
Z-0335-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
0 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): HYF-1T (04953170051128).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 10 of 22

Hysterovideoscope-For endoscopic diagnosis within the uterus Model Number: HYF-V.

Z-0336-2024
Recall number
Z-0336-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
27 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): HYF-V (04953170340185).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 11 of 22

Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number: HYF-XP.

Z-0337-2024
Recall number
Z-0337-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
16 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): HYF-XP (04953170340178).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 12 of 22

Tracheal fiberscope-airway management, which includes observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: LF-DP, LF-GP, LF-TP.

Z-0338-2024
Recall number
Z-0338-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
65 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): LF-DP (04953170136856), LF-GP (04953170061998), LF-TP (04953170317576).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 13 of 22

Tracheal videoscope- For airway management, which includes observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Number: LF-V.

Z-0339-2024
Recall number
Z-0339-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
61 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): LF-V (04953170340246)

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 14 of 22

Mobile airway scope-diagnosis and observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: MAF-DM2, MAF-GM, MAF-GM2, MAF-TM, MAF-TM2.

Z-0340-2024
Recall number
Z-0340-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
33 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Numbers: MAF-DM2 (04953170407260), MAF-GM (04953170340369), MAF-GM2 (04953170407208), MAF-TM (04953170288630), MAF-TM2 (04953170407147).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 15 of 22

Colonoscope-indicated for use within the lower digestive tract (including the anus, rectum, sigmoid colon, colon, and ileocecal valve). Model Numbers: PCF-H180AI, PCF-H180AL, PCF-H190DI, PCF-H190DL, PCF-H190I, PCF-H190L, PCF-H190TI, PCF-H190TL, PCF-HQ190I, PCF-HQ190L, PCF-PH190I, PCF-PH190L, PCF-Q180AI, PCF-Q180AL, PCF-S.

Z-0341-2024
Recall number
Z-0341-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
3101 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): PCF-H180AI (04953170339875), PCF-H180AL (04953170339899), PCF-H190DI (04953170363696), PCF-H190DL (04953170363672), PCF-H190I (04953170305214), PCF-H190L (04953170305191), PCF-H190TI (04953170420719), PCF-H190TL (04953170420702), PCF-HQ190I (04953170416132), PCF-HQ190L (04953170416118), PCF-PH190I (04953170305252), PCF-PH190L (04953170305238), PCF-Q180AI (04953170307713), PCF-Q180AL (04953170307720), PCF-S (04953170339912).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 16 of 22

Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum and sigmoid colon). Model Number: PCF-S.

Z-0342-2024
Recall number
Z-0342-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
8 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): PCF-S (04953170339912).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 17 of 22

Small intestinal videoscope-For endoscopy and endoscopic surgery within the upper digestive tract (including the esophagus, stomach, duodenum, and small intestine) by oral insertion or the lower digestive tract (including the anus, rectum, sigmoid colon, colon, ileocecal valve, and small intestine) by anal insertion. - Model Number: SIF-Q180.

Z-0343-2024
Recall number
Z-0343-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
32 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): SIF-Q180 (04953170339936)

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 18 of 22

Transnasal esophagovideoscope-For endoscopy and endoscopic surgery within the esophagus and stomach. Model Number: PEF-V.

Z-0344-2024
Recall number
Z-0344-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
25 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): PEF-V (04953170340376).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 19 of 22

Ultrasonic gastrovideoscope-Real time ultrasound imaging,ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs Model Number: TGF-UC180J.

Z-0345-2024
Recall number
Z-0345-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
5 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): TGF-UC180J (04953170328480).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 20 of 22

Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery Model Numbers: TJF-145, TJF-150, TJF-Q180V, TJF-Q190V.

Z-0346-2024
Recall number
Z-0346-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
0 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): TJF-145 (04953170339950), TJF-150 (04953170307553), TJF-Q180V (04953170229503), TJF-Q190V (04953170405563).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 21 of 22

Ureteralscope- for endoscopic diagnosis and treatment within the ureter, kidney and biliary tract (common bile duct and hepatic duct). Model Numbers: URF-P6, URF-P6R.

Z-0347-2024
Recall number
Z-0347-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
1577 units

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): URF-P6 (04953170340802), URF-P6R (04953170340833).

Distribution pattern

Worldwide - US Nationwide distribution.

device · product 22 of 22

Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-V3, URF-V3R.

Z-0348-2024
Recall number
Z-0348-2024
Initiated
September 25, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Aizu Olympus Co., Ltd.
Quantity
N/A

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
contamination that could lead

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information

Model Number (UDI-DI): URF-P7 (04953170403811), URF-P7R (04953170403835), URF-V2 (04953170343582), URF-V2R (04953170343612), URF-V3 (04953170403385), URF-V3R (04953170403392).

Distribution pattern

Worldwide - US Nationwide distribution.