Device recall: Rifton TRAM Standard Base, SKU K310, powered lift device
Class II FDA enforcement event 82607. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Class II, in the words of FDA
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
Community Products, LLC started this device recall on 21 Mar 2019. The firm address in the FDA record is in Rifton, NY. FDA put the recall in Class II. FDA event 82607 has 3 product records. The first FDA enforcement report date is 30 Oct 2019. The record gives the status Terminated, with the termination date 15 Jun 2020.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
The products were distributed US nationwide. The products were distributed to the following foreign countries: Foreign Countries: Worldwide, including Canada, United Kingdom, Germany, Japan,…
Recalling firm
Community Products, LLC, Rifton, NY.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
3 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0164-2020 | Rifton TRAM Standard Base, SKU K310, powered lift device | 3282 | Class II | Terminated | 30 Oct 2019 |
| Z-0165-2020 | Rifton TRAM Low Base, SKU K320, powered lift device | 1079 | Class II | Terminated | 30 Oct 2019 |
| Z-0166-2020 | Rifton E-Pacer, SKU K660, powered lift device | 167 | Class II | Terminated | 30 Oct 2019 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2019
- 968
- Share of these events in Class II
- 88%
- Product records in this event
- 3Median of the firm: 3
- Events of the firm on the register
- 2
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 18 Dec 2025 | Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seat | Device | Class II | 3 |
Official channels
- FDA enforcement report Z-0164-2020The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 82607. https://recallregister.com/fda/ii/82607/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
The products were distributed US nationwide. The products were distributed to the following foreign countries: Foreign Countries: Worldwide, including Canada, United Kingdom, Germany, Japan,…
- What quantity of product is in FDA event 82607?
- The event has 3 product records. The first record gives this quantity:
3282
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2019 have the same class?
- 88% of the 968 device events that started in 2019 are in Class II.