The Recall Desk

Hazard

Documentation Error recalls

426 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
426
Critical
0
Severe
0
Most recent
2026-09-02

Of the 426 documentation error recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all documentation error recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

126–150 of 426

  • LowFDA (Devices)·Z-3128-2017·2017-09-20

    Fujifilm ED-530XT Endoscope Manuals Recalled Following FDA Inspection

    Fujifilm is recalling 260 user manuals for the ED-530XT endoscope following an FDA inspection. The recall is a corrective action to address documentation issues.

    Product
    Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This product is not used for any other pur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1060-2017·2017-08-16

    AtHome Medical Recalls Liquid Oxygen Due to GMP Deviations

    AtHome Medical, Inc. is recalling 80 lbs of Oxygen Refrigerated Liquid USP due to a lack of standard operating procedures for testing out-of-specification products.

    Product
    Oxygen Refrigerated Liquid USP UN 1073, Rx only, At Home Medical 200 American Road, Morris Plains, NJ 07950,973-538-0485.
    Category
    Drug
    Distribution
    1 state
  • LowNHTSA·17V445000·2017-07-14

    Forest River Recalls 2017 Rockwood Travel Trailers for VIN Label Error

    Forest River is recalling 2017 Rockwood travel trailers because an incorrect check digit on the VIN label may hinder vehicle registration and safety recall tracking.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2666-2017·2017-07-12

    Exactech Equinoxe Modular Reverse Pilot-Tip Reamer Recall for Labeling Clarification

    Exactech is recalling Equinoxe Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.

    Product
    EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer, Catalog #: 321-25-38, Catalog #: 321-25-42 and Catalog #: 321-25-46
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Devices)·Z-2585-2017·2017-06-21

    Cook Inc. Recalls OptiLite Multi-Use Holmium Laser Fibers Due to Reprocessing Instructions

    Cook Inc. is voluntarily recalling OptiLite Multi-Use Holmium Laser Fibers because the reprocessing instructions lack sufficient detail for proper cleaning, disinfection, and sterilization.

    Product
    OptiLite Multi-Use Holmium Laser Fibers, Supplied sterilized by ethylene oxide gas in peel-open packages Product Usage: Used with the Odyssey 30 Holmium Laser System for fragmentation of urinary calculi and soft tissue applications including incision/excision, ablation, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2315-2017·2017-06-14

    Cook Medical Recalls LapSac Introducer Sets Due to Insufficient Reprocessing Instructions

    Cook Medical is voluntarily recalling 335 LapSac Introducer Sets because the provided reprocessing instructions lack sufficient detail for proper cleaning, disinfection, and sterilization.

    Product
    LapSac Introducer Set, Bag, Extraction, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to aid in the introduction of a LapSac during endoscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowNHTSA·17V352000·2017-05-31

    Volkswagen Recalls 2017 Jetta for VIN Marking Mismatch

    Volkswagen is recalling 2017 Jetta vehicles because the VIN on the body does not match the VIN plate near the windshield, violating federal certification regulations.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1987-2017·2017-05-10

    Anspach Effort 6.5cm Adult Cranial Thin Foot Plate Recall

    The Anspach Effort, Inc. is recalling 130 units of 6.5cm Adult Cranial Thin Foot Plates because the supplied directions for use did not contain a recommended service interval.

    Product
    6.5CM ADLT CRANI, THIN FT PLATE Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2022-2017·2017-05-10

    Anspach Effort Recalls 14cm QD Angle Attachment for Pneumatic Systems

    The Anspach Effort, Inc. is recalling 238 units of the 14cm QD Angle Attachment because the supplied directions for use did not contain a recommended service interval.

    Product
    14cm QD Angle Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1947-2017·2017-05-10

    Anspach Effort Recalls Electric Handpiece Controls for Missing Service Interval

    The Anspach Effort, Inc. is recalling 32 electric handpiece controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Electric Handpiece EM Hand Control Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1997-2017·2017-05-10

    Anspach Effort Recalls IMRI Short Attachment Pneumatic System Components

    The Anspach Effort, Inc. is recalling 14 IMRI Short Attachment units because the supplied directions for use did not include a recommended service interval.

    Product
    IMRI SHORT ATTACHMENT Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1937-2017·2017-05-10

    Anspach Effort Recalls Autolube-III Pneumatic Systems for Missing Service Interval

    The Anspach Effort, Inc. is recalling 17 Autolube-III pneumatic systems because the supplied directions for use did not include a recommended service interval.

    Product
    Autolube-III with Foot Guard Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1946-2017·2017-05-10

    Anspach Effort Electronic Foot Control Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 207 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2010-2017·2017-05-10

    Anspach Effort Recalls Minimal Access Attachments for Missing Service Interval

    The Anspach Effort, Inc. is recalling 22 Minimal Access Attachments because the supplied directions for use did not contain a recommended service interval.

    Product
    Minimal Access Attachment, BLACK MAX Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1954-2017·2017-05-10

    Anspach Effort SC2100 Foot Control Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 22 SC2100 foot controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Foot Control without Switches, SC2100 Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1980-2017·2017-05-10

    Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 297 pneumatic system attachments because the supplied directions for use did not include a recommended service interval.

    Product
    6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1953-2017·2017-05-10

    Anspach Effort SC2100 Foot Control Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 320 SC2100 Foot Controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Foot Control, SC2100 Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1945-2017·2017-05-10

    Anspach Effort Recalls XMAX Motor High Strength Hose for Missing Service Interval

    The Anspach Effort, Inc. is recalling 22 XMAX Motor High Strength Hoses because the supplied directions for use did not contain a recommended service interval.

    Product
    XMAX Motor, High Strength Hose Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1938-2017·2017-05-10

    Anspach Effort Recalls Autolube-III Pneumatic System for Missing Service Interval

    The Anspach Effort, Inc. is recalling 51 units of the Autolube-III with Irrigation pneumatic system because the supplied directions for use did not contain a recommended service interval.

    Product
    Autolube-III with Irrigation Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1930-2017·2017-05-10

    Anspach Effort Recalls 14cm QD Angle Attachment for Missing Service Interval

    The Anspach Effort, Inc. is recalling 14cm QD Angle Attachments because the supplied directions for use did not contain a recommended service interval.

    Product
    14cm QD Angle Attachment Product Usage: Product attachment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2012-2017·2017-05-10

    Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 8.0cm Medium Pneumatic System Attachments because the supplied directions for use did not contain a recommended service interval.

    Product
    8.0cm Medium Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1955-2017·2017-05-10

    Anspach Effort eMax2 Plus Console Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 439 eMax2 Plus consoles because the supplied directions for use did not contain a recommended service interval.

    Product
    Console, eMax2 Plus Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide