---
title: "Hobbs Medical, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search Hobbs Medical, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/hobbs-medical-inc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# Hobbs Medical, Inc. recall records

**72** reported ongoing

72 records in this archive. Latest source date Oct 4, 2024.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

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/).

## Records and reported status

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720](https://isitonrecall.com/recall/fda-device-z-0468-2025-posi-stop-injection-needle-23-gauge-catalog-number-4720/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0468-2025%22)

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702](https://isitonrecall.com/recall/fda-device-z-0469-2025-posi-stop-injection-needle-23-gauge-catalog-number-4702/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0469-2025%22)

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706](https://isitonrecall.com/recall/fda-device-z-0470-2025-posi-stop-injection-needle-23-gauge-catalog-number-4706/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0470-2025%22)

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716](https://isitonrecall.com/recall/fda-device-z-0471-2025-posi-stop-injection-needle-23-gauge-catalog-number-4716/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0471-2025%22)

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721](https://isitonrecall.com/recall/fda-device-z-0472-2025-posi-stop-injection-needle-23-gauge-catalog-number-4721/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0472-2025%22)

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704](https://isitonrecall.com/recall/fda-device-z-0473-2025-posi-stop-injection-needle-25-gauge-catalog-number-4704/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0473-2025%22)

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718](https://isitonrecall.com/recall/fda-device-z-0474-2025-posi-stop-injection-needle-25-gauge-catalog-number-4718/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0474-2025%22)

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722](https://isitonrecall.com/recall/fda-device-z-0475-2025-posi-stop-injection-needle-25-gauge-catalog-number-4722/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0475-2025%22)

Oct 4, 2024 FDA device enforcement

### [Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723](https://isitonrecall.com/recall/fda-device-z-0476-2025-posi-stop-injection-needle-25-gauge-catalog-number-4723/)

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

[Official source for Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0476-2025%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190](https://isitonrecall.com/recall/fda-device-z-0010-2023-hobbs-medical-spray-catheter-the-mistifier-2-6mm-260cm-disposable-for-endoscopy-procedures-ref-2190/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref:...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0010-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 165cm Disposable For endoscopy procedures Ref: 2191](https://isitonrecall.com/recall/fda-device-z-0011-2023-hobbs-medical-spray-catheter-the-mistifier-2-6mm-165cm-disposable-for-endoscopy-procedures-ref-2191/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 165cm Disposable For endoscopy procedures Ref:...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0011-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412](https://isitonrecall.com/recall/fda-device-z-0012-2023-hobbs-medical-flex-ez-guide-wire-disposable-for-endoscopy-procedures-ref-3412/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0012-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Medical Cytology Brush Catalog Number: 4204](https://isitonrecall.com/recall/fda-device-z-0013-2023-hobbs-medical-cytology-brush-catalog-number-4204/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Medical Cytology Brush Catalog Number: 4204](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0013-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Medical Cytology Brush Catalog Number: 4206](https://isitonrecall.com/recall/fda-device-z-0014-2023-hobbs-medical-cytology-brush-catalog-number-4206/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Medical Cytology Brush Catalog Number: 4206](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0014-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Medical Polypectomy Snare Catalog Number: 4563](https://isitonrecall.com/recall/fda-device-z-0015-2023-hobbs-medical-polypectomy-snare-catalog-number-4563/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Medical Polypectomy Snare Catalog Number: 4563](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0015-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Medical Polypectomy Snare Catalog Number: 4564](https://isitonrecall.com/recall/fda-device-z-0016-2023-hobbs-medical-polypectomy-snare-catalog-number-4564/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Medical Polypectomy Snare Catalog Number: 4564](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0016-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620](https://isitonrecall.com/recall/fda-device-z-0017-2023-hobbs-transbronchial-aspiration-needle-and-vacu-lok-aspirating-syringe-catalog-number-4620/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0017-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Transbronchial Aspiration Needle Catalog Number: 4621](https://isitonrecall.com/recall/fda-device-z-0018-2023-hobbs-transbronchial-aspiration-needle-catalog-number-4621/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Transbronchial Aspiration Needle Catalog Number: 4621](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0018-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Scope Introducer Catalog Number: 4650](https://isitonrecall.com/recall/fda-device-z-0019-2023-hobbs-scope-introducer-catalog-number-4650/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Scope Introducer Catalog Number: 4650](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0019-2023%22)

Jul 29, 2022 FDA device enforcement

### [Hobbs Posi-Stop Injection Needle Catalog Number: 4702](https://isitonrecall.com/recall/fda-device-z-0020-2023-hobbs-posi-stop-injection-needle-catalog-number-4702/)

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in ...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

[Official source for Hobbs Posi-Stop Injection Needle Catalog Number: 4702](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0020-2023%22)

## Reasons in these listed records

- Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits conta...

These examples come from this result page and are not a ranking of every recall reason.

## Checking Hobbs Medical, Inc.

### Is there a recall on hobbs medical, inc. right now?

This archive contains 72 records, including 72 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search Hobbs Medical, Inc.](https://isitonrecall.com/check/?q=Hobbs%20Medical%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
