Prism Medical P-600 Portable Ceiling Lift Recalled for Sling Attachment Risk
Prism Medical is recalling 409 P-600 Portable Ceiling Lifts because sling loops may not stay attached to the carry bar hooks.
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 risk-of-harm product (patient lift) where injury has not yet been reported, fitting the 'High' severity criteria for potential physical injury without confirmed cases.
Plain-English summary
ErgoSafe Products, LLC (DBA Prism Medical) is recalling 409 units of the Prism Medical P-600 Portable Ceiling Lift (PN 303090). The recall is due to a potential safety issue where the sling loops may not stay attached to the carry bar hooks.
The affected lifts are used by health care professionals and caregivers to lift, position, and transfer clients or disabled family members. The product was distributed worldwide, including the United States, Canada, Great Britain, Australia, South Korea, and Japan. All serial numbers are included in this recall.
Consumers should stop using the affected lifts and contact the recalling firm for instructions on how to proceed.
The recalled product
- Product
- Prism Medical P-600 Portable Ceiling Lift; PN 303090. Patient lift with weight specification of 600 lbs (273 kg). Product Usage: The P-600 lift is a lifting aid used by health care professionals and those providing care in the home to lift, position, and transfer clients…
- Manufacturer
- ErgoSafe Products, LLC (DBA) Prism Medical
- Category
- Medical Device — Patient Lift
- Affected units
- 409
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)
- All serial numbers.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by ErgoSafe Products, LLC (DBA) Prism Medical under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
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