PlainRecalls

Hobbs Medical, Inc.

Compiled from official public sources by the editorial team.

73 recalls on record · Latest: Nov 27, 2024

Hobbs Medical, Inc. Recall Insight

Hobbs Medical, Inc. appears on 73 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.072% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Nov 27, 2024, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 23 entries, severity tagging shows 0 critical, 23 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 23 of 23 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (23). The date window on this page runs from Jun 13, 2018 to Oct 19, 2022.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Oct 19, 2022

Hobbs Helical Retrieval Basket Catalog Number: 4830

FDA Devices Moderate Oct 19, 2022

Hobbs Retrieval Forceps Catalog Number: 5018

FDA Devices Moderate Oct 19, 2022

Hobbs Medical Polypectomy Snare Catalog Number: 4564

FDA Devices Moderate Oct 19, 2022

Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352

FDA Devices Moderate Oct 19, 2022

Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6351

FDA Devices Moderate Oct 19, 2022

Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004

FDA Devices Moderate Oct 19, 2022

Freeman Pancreatic Flexi-Stent Catalog Number: 6535

FDA Devices Moderate Oct 19, 2022

Hobbs Scope Introducer Catalog Number: 4650

FDA Devices Moderate Oct 19, 2022

Hobbs Medical Polypectomy Snare Catalog Number: 7202

FDA Devices Moderate Oct 19, 2022

Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024

FDA Devices Moderate Oct 19, 2022

Hobbs Helical Retrieval Basket Catalog Number: 4814

FDA Devices Moderate Oct 19, 2022

Hobbs Biliary Pigtail Stent Kits Catalog Number: 6105

FDA Devices Moderate Oct 19, 2022

Hobbs Posi-Stop Injection Needle Catalog Number: 4720

FDA Devices Moderate Oct 19, 2022

Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544) Catalog Number: 6503

FDA Devices Moderate Oct 19, 2022

Hobbs Biliary Pigtail Stent Kits (containing 6105) Catalog Number: 6023

FDA Devices Moderate Oct 19, 2022

Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412

FDA Devices Moderate Oct 19, 2022

Hobbs Medical Polypectomy Snare Catalog Number: 4563

FDA Devices Moderate Oct 19, 2022

Hobbs Posi-Stop Injection Needle Catalog Number: 4712

FDA Devices Moderate Oct 19, 2022

Freeman Pancreatic Flexi-Stent Catalog Number: 6566

FDA Devices Moderate Oct 19, 2022

Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028

FDA Devices Moderate Jul 27, 2022

Hobbs Medical Polypectomy Snare, Catalog No. 7202

FDA Devices Moderate Mar 9, 2022

Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as the base of brush wire to expo…

FDA Devices Moderate Jun 13, 2018

Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained personnel through a flexible …

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.