PlainRecalls

Hill-Rom, Inc.

23 recalls on record · Latest: Mar 23, 2022

Hill-Rom, Inc. Recall Insight

Hill-Rom, Inc. appears on 23 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.027% 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 Mar 23, 2022, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 23 entries, severity tagging shows 1 critical, 22 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 Jul 4, 2012 to Mar 23, 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 Mar 23, 2022

(1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko overhead lift…

FDA Devices Moderate Feb 23, 2022

Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015

FDA Devices Moderate Dec 29, 2021

These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call, Part Number 4.0 *Produ…

FDA Devices Moderate Oct 6, 2021

LikoStretch Mod 600 IC Model Number: 3156065 LikoStretch Mod 600 IC, Wide Model Number: 3156065B (obsolete since 12JUN2020) - The combination of thi…

FDA Devices Moderate Oct 6, 2021

LikoStretch 1900 Model Number: 3156051 - The combination of this products allows the user to easily adjust/control the center of gravity during lift …

FDA Devices Moderate Oct 6, 2021

Stretch Leveller Model Number: 3156200 - The combination of this products allows the user to easily adjust/control the center of gravity during lift …

FDA Devices Critical Feb 10, 2021

Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. A…

FDA Devices Moderate Aug 5, 2020

Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility…

FDA Devices Moderate Jun 10, 2020

Centrella Smart+ Bed, Catalog Number P7900

FDA Devices Moderate Apr 18, 2018

Progressa Bed - AC-powered adjustable hospital bed

FDA Devices Moderate Sep 14, 2016

Affinity Four Birthing Bed Model P3700 The primary packaging is pictured below, and utilizes a metal packing brace, standard corrugated cardboar…

FDA Devices Moderate Aug 17, 2016

Volker 2080, 2082, S 280 and S 282 series beds with lateral release button. A/C Powered Adjustable Hospital Bed Product Usage: Volker model 2080…

FDA Devices Moderate Nov 25, 2015

Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed

FDA Devices Moderate Jul 1, 2015

Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.

FDA Devices Moderate Jun 24, 2015

Viking M, L, and XL Mobile Lifts. Non-AC-powered patient lift.

FDA Devices Moderate Sep 10, 2014

Affinity¿ Four Birthing Bed, Product Usage: Product is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Del…

FDA Devices Moderate Jul 31, 2013

TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum Complete mattress, and AccuMax Quantum Convertible mattress The TotalCare Be…

FDA Devices Moderate Jun 12, 2013

SlingBar 350. Designed to meet the needs for lifting humans.

FDA Devices Moderate Jun 12, 2013

SlingBar Standard. Designed to meet the needs for lifting humans.

FDA Devices Moderate Mar 20, 2013

TotalCare SpO2RT2 bed. Product Usage: Bed, flotation therapy, powered bed may be used in a variety of settings including, but not limited to, …

FDA Devices Moderate Feb 27, 2013

Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and Masterlift Systems Produ…

FDA Devices Moderate Aug 1, 2012

Affinity Four Birthing Bed P3700 Product Usage: The Affinity, Four Birthing Bed is intended to be used as birthing beds for women of child beari…

FDA Devices Moderate Jul 4, 2012

Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital.

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

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