Lower riskMedical device recall · FDA · Published February 1, 2022
BSN Medical JOBST Compri2 Recalls Mislabeling in Shipping Boxes
BSN Medical recalls JOBST Compri2 and lite products due to mislabeled shipping boxes. The hazard involves incorrect labeling of folding boxes within the shipping case, which may cause confusion during use.
“BSN Medical JOBST Compri2 Recalls Mislabeling in Shipping Boxes.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61194-bsn-medical-jobst-compri2-recalls-mislabeling-in-shipping-boxes. Based on FDA recall #Z-1228-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1228-2022%22&limit=1).
The Food and Drug Administration announced on Feb. 1, 2022, that BSN Medical Inc is recalling JOBST Compri2 and JOBST Compri2 lite compression bandages because the folding boxes within the shipping case are mislabeled. The agency said the recall involves approximately 1,677 units distributed nationwide.
How to tell if you have it
JOBST Compri2, REF 76271-01
JOBST Compri2 lite, REF 76271-02
Lot #127384
Expiration date: 2024-02-10
UPC 04042809506631
UPC 04042809506648
The hazard
The folding boxes within the shipping case are mislabeled, according to the FDA. The shipping case and immediate packages within the folding boxes are correctly labeled.
Context
GovInfoNow's records show BSN Medical has had other recent recalls of similar products include JOBST Compri2 (2022-02-01). Other recent recalls of similar products include Covidien Shiley Tracheostomy Tube Recall: Incorrect Box Labeling (2026-04-15), Omnicell i.v.Station Label Stock Recall: Risk of Mislabeled Syringes (2026-03-25), and Blom-Singer Classic Voice Prosthesis Recall: Incorrect Labeling Hazard (2026-06-17).
How to tell if you have this one
Check for the product name and lot number on the shipping case. The recalled products include JOBST Compri2 (REF 76271-01) and JOBST Compri2 lite (REF 76271-02), with lot number 127384 and expiration date 2024-02-10.
Brand
BSN Medical
Product
(1) JOBST Compri2, REF 76271-01, containing 2 components, one plastic-wrapped padding and one plastic-wrapped
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Labels
Look for the product name and lot number on the shipping case to confirm if it is part of the recall.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 15 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of AZ, FL, CA, IL, KS, MA, MN, MO, NC, NH, OH, PA, TX, VA, and WA. There was no foreign/government/military distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Florida, Illinois, Kansas, Massachusetts, Minnesota, Missouri, New Hampshire, North Carolina, Ohio, Pennsylvania, Texas, Virginia, Washington.
Recall timeline
FDA terminated this recall 18 months 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-1228-2022 (February 1, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1228-2022 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.