---
title: "11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (... — FDA record Z-1054-2022 | Is It on Recall"
description: "Failure to achieve the expected six-log reduction in microorganisms following the disinfection process."
url: https://isitonrecall.com/recall/fda-device-z-1054-2022-11001rd1-11001rdk1-karl-storz-slim-nasopharyngolaryngoscope-96216006us-v5-0-10-2018/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018) — FDA record Z-1054-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 1, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018)
- **Reason**: Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.
- **Classification**: Class II
- **Recalling firm**: Karl Storz Endoscopy
- **Quantity**: All Serial Numbers manufactured/distributed since January 2018
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1054-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1054-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018) UDI Code: 0408551225608 All Serial Numbers manufactured/distributed since January 2018 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

U.S. Nationwide distribution in the states of FL, KY, LA, MA, MI, MO, MT, NC, NH, NJ, OK, SC, TX and WA.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Indiana](https://isitonrecall.com/state/indiana/)
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- [Nevada](https://isitonrecall.com/state/nevada/)
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- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: May 18, 2022
- **Recall initiation date**: Apr 1, 2022
- **Center classification date**: May 10, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1054-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Karl Storz Endoscopy records](https://isitonrecall.com/brand/karl-storz-endoscopy/)
