Use cautionMedical device recall · FDA · Published March 6, 2020
R82 Chest Support and Rabbit Up Recalls: Plastic Plug Can Come Loose
R82 A/S recalls chest supports for Mustang and Rabbit Up models (2017-2020) due to plastic plug potentially coming loose without tools. Affected units include specific model numbers.
“R82 Chest Support and Rabbit Up Recalls: Plastic Plug Can Come Loose.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65701-r82-chest-support-and-rabbit-up-recalls-plastic-plug-can. Based on FDA recall #Z-1858-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1858-2020%22&limit=1).
The FDA announced on March 6, 2020, that R82 A/S is recalling Chest Support for R82 Mustang and Rabbit Up units due to a loose plastic plug hazard. The agency issued recall number Z-1858-2020 for the voluntary Class II recall.
How to tell if you have it
Brand: R82 A/S
Product: Chest Support for R82 Mustang, Model Numbers: 861810, 861820, 861830
Product: Rabbit Up, Model Numbers: 869810, 869820, 869830
Distribution: North Carolina
Units affected: 2230
The hazard
The plastic plug on the chest support for Mustang and Rabbit/Rabbit Up can come loose without use of a tool, according to the FDA.
Context
GovInfoNow's records show R82 A/S has 3 other recalls on record since June 30, 2017. Other recent recalls include the ETAC R82 Push Brace for High-Low (Dec. 8, 2021), Wombat Living Size 3 Activity Chair (March 28, 2019), and Heron Model 880505 Toilet and Bath Chair (June 30, 2017).
How to tell if you have this one
Check your chest support model number: Mustang models are 861810-861830, Rabbit Up models are 869810-869830. The product was sold between April 2017 and February 2020.
Brand
R82 A/S
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Model Number
Look for the model number on your chest support: Mustang models are 861810-861830, Rabbit Up models are 869810-869830.
Contact Manufacturer
Reach out to R82 A/S for further instructions on how to address the issue.
Where it went and when
Where it was distributed
Distributed in North Carolina.
Listed by the agency
Not listed
FDA distribution: “NC” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: North Carolina.
Recall timeline
FDA terminated this recall 3.5 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1858-2020 (March 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1858-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.