Prism Medical C-Series Carry Bar Recalled for Improper Installation
Prism Medical Services USA is recalling 1,131 C-Series Carry Bars due to improper installation. The firm is replacing them with a plastic insert and metal insert carry bar.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device used for patient lifting where improper installation poses a risk of harm, but the source text does not report any specific injuries or illnesses.
Plain-English summary
Prism Medical Services USA is recalling the Prism Medical C-Series Carry Bar, Class I, model number 360755. The intended use of this product is as a carry bar attached to a C-450 or C-625 ceiling lift used to lift, transfer, or position clients.
The recall is being conducted due to improper installation of the recalled carry bars. The firm is replacing the recalled carry bar with a plastic insert with a carry bar with a metal insert.
A total of 1,131 carry bars were distributed in the United States (nationwide) and Canada. Consumers should contact the firm for replacement.
The recalled product
- Product
- Prism Medical C-Series Carry Bar, Class I, model number 360755. The intended use is a carry bar attached to a C-450 or C-625 ceiling lift used to lift, transfer or position clients.
- Manufacturer
- Prism Medical Services USA
- Category
- Medical Device — Ceiling Lifts
- Hazard
- Affected units
- 1,131
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- model number 360755
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · Prism Medical Services USA
See all →- LowPrism Medical Recalls BC Hammock Mesh Slings Due to Incorrect Size
FDA (Devices) · 2013-06-26
- LowPrism Medical BC Hammock Mesh Sling Recalled for Incorrect Size
FDA (Devices) · 2013-06-26
- ModeratePrism Medical Recalls BC Hammock Mesh Slings Due to Incorrect Size
FDA (Devices) · 2013-06-26
- ModeratePrism Medical Recalls BC Hammock Mesh Sling for Incorrect Size
FDA (Devices) · 2013-06-26
Same hazard · improper installation
See all →- High2026 Forest River Sabre Fifth Wheel Griddle Fire Risk Recall
NHTSA · 2025-06-20
- High
- Severe2022-2025 Rivian R1T and R1S recalled for unsecured seat belt anchors
NHTSA · 2025-06-03
- HighNova Bus recalls 2022-2024 LFS buses for wheelchair restraint defect
NHTSA · 2024-12-03
- HighPhilips Evolution 3.0T MRI System patient table floor plate installation defect
FDA (Devices) · 2024-04-24
Similar recalls
- HighPrism Medical Carry Bar Recall Due to Breaking Plastic Component
FDA (Devices) · 2016-12-21
- HighPrism Medical P-600 Portable Ceiling Lift Recalled for Sling Attachment Risk
FDA (Devices) · 2015-08-05
- SeverePrism Medical C-300 Ceiling Lifts Recalled for Drive Shaft Failure
FDA (Devices) · 2015-11-25
- HighPrism Medical P-440 Portable Ceiling Lift Recalled for Sling Attachment Risk
FDA (Devices) · 2015-08-05
- SeverePrism Medical P-300 Portable Consumer Lift Recalled for Drive Shaft Failure
FDA (Devices) · 2015-11-25
- HighHandicare C Series Patient Lifts Recalled for Premature Strap Wear
FDA (Devices) · 2018-08-29