CLASS II ONGOING Device recall · Reported 28 Jan 2026 · FDA Enforcement Report

Rifton Equipment, Low Base TRAM recalled by Community Products

Community Products is recalling Rifton Equipment, Low Base TRAM, distributed nationwide in the US. The recall was initiated on 18 Dec 2025 and the FDA has classified it as Class II.

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Lot, batch or date codesModel/Catalog Number: K320. ID Codes: K32020130515AA, K32020130603AA, K32020130606AA, K32020130607AB, K32020130610AA, K32020130612AA, K32020130617AA, K32020130617AB, K32020130618AA, K32020130709AA, K32020130713AA, K32020130713AB, K32020130717AB, K32020130802AA, K32020130805AA, K32020130807AA, K32020130808AA, K32020130808AB, K32020130812AA, K32020130812AB, K32020130812AC, K32020130812AD, K32020130813AA, K32020130814AA, K32020130820AA, K32020130822AA, K32020130823AA, K32020130824AA, K32020130827AA, K32020130827AB, K32020130828AA, K32020130830AA, K32020130907AA, K32020130909AB, K32020130909AC, K32020130909AD, K32020130909AE, K32020130919AA, K32020130920AA, K32020130924AA, K32020131007AA, K32020131007AB, K32020131009AA, K32020131017AB, K32020131021AA, K32020131022AB, K32020131022AC, K32020131022AD, K32020131024AA, K32020131025AA, K32020131029AA, K32020131031AA, K32020131101AA, K32020131102AA, K32020131107AA, K32020131115AD, K32020131119AA, K32020131120AD, K32020131205AA, K32020131210AA, K32020131217AD, 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Quantity recalled1,096 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1138-2026
FDA event ID: 98140
Recalling firm: Community Products, Rifton, NY
Classification: Class II
Status: Ongoing
Recall initiated: 18 Dec 2025
FDA classified: 22 Jan 2026
Reported: 28 Jan 2026
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

18 Dec 2025	Recall initiated by company
22 Jan 2026	Classified by FDA	+35 days
28 Jan 2026	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential for fraying on the body support strap.

Product as listed by the FDA

Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training. The low base variant includes smaller casters and lower base frame so that the legs fit underneath beds.

Where it was distributed

Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.

Nationwide

Questions about this recall

Why was it recalled?

Potential for fraying on the body support strap.

Which lots are affected?

Model/Catalog Number: K320. ID Codes: K32020130515AA, K32020130603AA, K32020130606AA, K32020130607AB, K32020130610AA, K32020130612AA, K32020130617AA, K32020130617AB, K32020130618AA, K32020130709AA, K32020130713AA, K32020130713AB, K32020130717AB, K32020130802AA, K32020130805AA, K32020130807AA, K32020130808AA, K32020130808AB, K32020130812AA, K32020130812AB, K32020130812AC, K32020130812AD, K32020130813AA, K32020130814AA, K32020130820AA, K32020130822AA, K32020130823AA, K32020130824AA, K32020130827AA, K32020130827AB, K32020130828AA, K32020130830AA, K32020130907AA, K32020130909AB, K32020130909AC, K32020130909AD, K32020130909AE, K32020130919AA, K32020130920AA, K32020130924AA, K32020131007AA, K32020131007AB, K32020131009AA, K32020131017AB, K32020131021AA, K32020131022AB, K32020131022AC, K32020131022AD, K32020131024AA, K32020131025AA, K32020131029AA, K32020131031AA, K32020131101AA, K32020131102AA, K32020131107AA, K32020131115AD, K32020131119AA, K32020131120AD, K32020131205AA, K32020131210AA, K32020131217AD, K32020140103AA, K32020140113AA, K32020140115AA, K32020140117AA, K32020140121AA, K32020140122AA, K32020140122AB, K32020140125AA, K32020140130AB, K32020140210AA, K32020140218AA, K32020140218AB, K32020140220AA, K32020140221AA, K32020140224AA, K32020140304AA, K32020140305AB, K32020140312AA, K32020140315AA, K32020140327AA, K32020140327AC, K32020140401AA, K32020140407AA, K32020140407AB, K32020140408AA, K32020140412AA, K32020140415AA, K32020140417AA, K32020140422AA, K32020140423AA, K32020140426AA, K32020140429AA, K32020140514AB, K32020140516AA, K32020140516AB, K32020140519AA, K32020140519AB, K32020140520AA, K32020140520AB, K32020140523AA, K32020140528AA, K32020140528AB, K32020140530AA, K32020140530AB, K32020140530AC, K32020140604AA, K32020140607AA, K32020140619AA, K32020140619AB, K32020140620AB, K32020140624AB, K32020140626AA, K32020140711AB, K32020140712AA, K32020140719AA, K32020140721AA, K32020140722AA, K32020140722AB, K32020140725AA, K32020140728AA, K32020140730AC, K32020140802AA, K32020140805AA, K32020140812AA, K32020140812AB, K32020140815AA, K32020140827AA, K32020140902AA, K32020140906AA, K32020140913AB, K32020140915AB, K32020140917AA, K32020140918AA, K32020140923AA, K32020140923AB, K32020140924AA, K32020140929AA, K32020140930AA, K32020141006AA, K32020141006AB, K32020141006AC, K32020141008AA, K32020141014AA, K32020141021AA, K32020141028AA, K32020141030AA, K32020141031AA, K32020141101AB, K32020141107AA, K32020141107AB, K32020141113AA, K32020141113AB, K32020141118AD, K32020141120AA, K32020141121AA, K32020141121AB, K32020141124AA, K32020141128AA, K32020141203AA, K32020141209AA, K32020141209AC, K32020141213AA, K32020141215AA, K32020141215AB, K32020141215AC, K32020141215AD, K32020141229AA, K32020141229AB, K32020141229AC, K32020150102AA, K32020150112AA, K32020150123AA, K32020150128AA, K32020150128AB, K32020150128AC, K32020150129AA, K32020150130AA, K32020150130AB, K32020150130AC, K32020150202AA, K32020150203AA, K32020150207AB, K32020150207AC, K32020150211AA, 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Where was it sold?

Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 98140

This product is part of a recall event; the main page for the event is Rifton Equipment, TRAM recalled by Community Products.

Reported	Class	Recall	Company	Reason	Where
28 Jan 2026	CLASS II	Rifton Equipment, TRAM recalled by Community Products	Community Products	Other	Nationwide
28 Jan 2026	CLASS II	Rifton Equipment, E-Pacer recalled by Community Products	Community Products	Other	Nationwide

More recalls from Community Products

All 6

Reported	Class	Recall	Company	Reason	Where
28 Jan 2026Device	CLASS II	Rifton Equipment, E-Pacer recalled by Community Products	Community Products	Other	Nationwide
28 Jan 2026Device	CLASS II	Rifton Equipment, TRAM recalled by Community Products	Community Products	Other	Nationwide
30 Oct 2019Device	CLASS II	Rifton E-Pacer recalled by Community Products	Community Products	Device Malfunction	Nationwide
30 Oct 2019Device	CLASS II	Rifton TRAM Low Base recalled by Community Products	Community Products	Device Malfunction	Nationwide
30 Oct 2019Device	CLASS II	Rifton TRAM Standard Base recalled by Community Products	Community Products	Device Malfunction	Nationwide

Other Other Medical Devices recalls

All 13,908

Reported	Class	Recall	Company	Reason	Where
14 Oct 2026Device	CLASS II	Plastics Tray kits recalled by Avid Medical	Avid Medical	Foreign Material	Nationwide
14 Oct 2026Device	CLASS II	Heart Prep Tray kits recalled by Avid Medical	Avid Medical	Other	Nationwide
14 Oct 2026Device	CLASS II	Pack Open Heart Cfh kits recalled by Avid Medical	Avid Medical	Other	Nationwide
14 Oct 2026Device	CLASS II	Sperm Ab Elisa (96 well plate test) recalled by DRG International	DRG International	Other	Nationwide
14 Oct 2026Device	CLASS III	BeneView Series recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide