PlainRecalls

Arjohuntleigh Polska Sp. z.o.o.

Compiled from official public sources by the publisher.

11 recalls on record · Latest: Apr 22, 2026

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Agency notice ledger

Federal filing book Arjohuntleigh Polska Sp. z.… LIGHT-BOOK · SINGLE-AGENCY

#1,317 of 14,151 · 11 notices · 0.011% archive

  • BOOK 11 notices
  • RANK #1,317 of 14,151
  • SHARE 0.011% archive
  • AGENCY FDA Devices (11)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 22, 2026
  • PHOTO Agfa Corp.

Nearest notice-volume peer: Agfa Corp. (0 notice gap)

Arjohuntleigh Polska Sp. z.o.o. accounts for about 0.011% of the 104,423-notice archive on 11 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Arjohuntleigh Polska Sp. z.… compares to 14,151 recalling firms

Arjohuntleigh Polska Sp. z.o.o. ranks 1,317th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Arjohuntleigh Polska Sp. z.… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

11 1317th of 14151 higher than 12,735 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Arjohuntleigh Polska Sp. z.… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Arjohuntleigh Polska Sp. z.o.o. holds about 0.011% of archive notices alongside 11 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Apr 22, 2026

Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
FDA Devices Moderate Jan 3, 2024

Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assistance modules
FDA Devices Moderate Jan 3, 2024

Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assistance modules
FDA Devices Critical Jun 1, 2022

Sara Plus Active Floor Lift
FDA Devices Moderate Oct 6, 2021

Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0; and IndiGo modules (retrofit kits) that can be installed on Citadel (model no. INDIDAA) or Enterprise (model no. INDIJAA) beds manufactured without IndiGo modules assembled at the time of manufacturing and subsequently retrofitted on the beds.
FDA Devices Moderate Aug 26, 2020

Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care environments. It is not intended for use in the home care environment.
FDA Devices Moderate Mar 18, 2020

Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102 [(01)05056097364483], BAB1007-01 [(01)05055982796255], BAB1101-01 [(01)05055982787949], BAB1102-01 [(01)05055982796156], BAB1103-01 [UDI: (01)05055982796163], BAB1107-01 [(01)05055982796187], BAB2000-01 [UDI: (01)05055982788106], BAB2101-01 [(01)05055982788007], BAB2102-01 [01)05055982796194], BAB3000-01 [(01)05055982788120], BAB3101-01 [(01)05055982788021], BAB3107-01[ (01)05055982796248], BAB500
FDA Devices Moderate Dec 19, 2018

ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage: The Arjo Passive Clip Sling is a product intended for assisted transfer of patient/resident with limited ability to move. Designed to be used for one patient during hospital stay and assists the caregiver with everyday patient handling routines, such as bed and chair related transfers. REF MFA1000M-L-L1 RM0255_7
FDA Devices Moderate Sep 14, 2016

ArjoHuntleigh Sara Combilizer; Intended to facilitate early immobilization, rehabilitation, and care of patients.
FDA Devices Moderate Oct 1, 2014

Minstrel (with scale) Product Usage: is a mobile passive hoist. It is intended for lifting and transporting adult residents on horizontal floors in hospitals, nursing homes or other health care facilitates. The Minstrel device aids in the lifting, transfer and lowering to safe position, of a patient. This is accomplished by placing a sling under the patient, and attaching the sling to a spreader bar that is connected to a lifting arm jig via a connection to the spreader bar that allows a swi
FDA Devices Moderate Sep 24, 2014

Tenor is a mobile passive lift, intended to be used on horizontal surfaces for lifting and transfer in hospitals, nursing homes or other healthcare facilities. Transfers with the Tenor are made indoors in the patient's room, in communal areas or in a bathroom. Tenor is meant to be used with the patient type who: sits in a wheelchair, has no capability to support themselves at all, cannot stand unsupported and is not able to bear weight (not even partially), is dependent on caregiver in most situ

Arjohuntleigh Polska Sp. z.… holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (11 here — thin-book).

Agfa Corp. 11 Ajinomoto Foods North America Inc. 11 Akron Pharma, Inc. 11 Amendia, Inc 11 Aniara Diagnostica LLC 11

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Agfa Corp. 11 Amendia, Inc 11 Aniara Diagnostica LLC 11 Caire, Inc. 11

Frequently Asked Questions

How many federal recall notices name Arjohuntleigh Polska Sp. z.…? ▼
PlainRecalls indexes 11 distinct federal recall events naming Arjohuntleigh Polska Sp. z.o.o., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Arjohuntleigh Polska Sp. z.… sit among other recalling firms? ▼
Arjohuntleigh Polska Sp. z.o.o. ranks #1,317 of 14,151 by distinct recall-event count among 14,151 firms in this archive (90th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Arjohuntleigh Polska Sp. z.…'s notices? ▼
FDA Devices accounts for 11 of this firm's 11 indexed notices.
What product category dominates Arjohuntleigh Polska Sp. z.…'s filing book? ▼
Filings for Arjohuntleigh Polska Sp. z.o.o. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Arjohuntleigh Polska Sp. z.o.o.: 11 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Arjohuntleigh Polska Sp. z.o.o.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026