Hobbs Medical, Inc.
Complete recall history across all FDA and CPSC categories — 73 total recalls
Hobbs Medical, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (73)
FDA medical device enforcement actions by Hobbs Medical, Inc.. Showing most recent 50.
| Date | Product | Reason | Class |
|---|---|---|---|
| Oct 4, 2024 | Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Oct 4, 2024 | Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Oct 4, 2024 | Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Oct 4, 2024 | Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Oct 4, 2024 | Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Oct 4, 2024 | Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Oct 4, 2024 | Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Oct 4, 2024 | Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Oct 4, 2024 | Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723 | Injection solutions would not flow as intended through the tip of 25ga-sized ... | Class II |
| Jul 29, 2022 | Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6566 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Posi-Stop Injection Needle Catalog Number: 4712 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Medical Polypectomy Snare Catalog Number: 4563 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref:... | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Biliary Pigtail Stent Kits (containing 6105) Catalog Number: 6023 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544) Catal... | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Posi-Stop Injection Needle Catalog Number: 4720 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Biliary Pigtail Stent Kits Catalog Number: 6105 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Helical Retrieval Basket Catalog Number: 4814 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Medical Polypectomy Snare Catalog Number: 7202 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Scope Introducer Catalog Number: 4650 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6535 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6351 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Medical Polypectomy Snare Catalog Number: 4564 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Retrieval Forceps Catalog Number: 5018 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Helical Retrieval Basket Catalog Number: 4830 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6534 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Medical Grasping Forceps Catalog Number: 5008 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Kit (containing 6566) Catalog Number: 6518 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Medical Polypectomy Snare Catalog Number: 4563-OLY | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Kit (containing 6567) Catalog Number: 6519 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Biliary Pigtail Stent Kits Catalog Number: 6104 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Posi-Stop Injection Needle Catalog Number: 4704 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Helical Retrieval Basket Catalog Number: 4816 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6562 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endo... | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Helical Retrieval Basket Catalog Number: 4808 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6567 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Cat... | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent (contained in kit 6501) Catalog Number: 6541 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6582 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6568 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Helical Retrieval Basket Catalog Number: 4824 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6544 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Hobbs Biliary Pigtail Stent Kits Catalog Number: 6108 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
| Jul 29, 2022 | Freeman Pancreatic Flexi-Stent Catalog Number: 6548 | Device label display an incorrect expiration date, extends the shelf life of ... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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