Medline Recalls CURAD Reusable Gel Hot/Cold Packs for Latex Mislabeling
Medline recalls CURAD reusable gel hot/cold packs that falsely claim no natural rubber latex. These packs may cause allergic reactions if the label is misleading.
Lower-risk recall
The product contains natural rubber latex but the label states that it does not.
Contact the company
What happened, in plain English
Medline is recalling CURAD reusable gel hot/cold packs because they contain natural rubber latex despite labeling as latex-free. This could cause allergic reactions in sensitive individuals. Read more at govinfonow.com/recall/61430-medline-recalls-curad-reusable-gel-hot-cold-packs-for-latex.
Source Summary by GovInfoNow · govinfonow.com/recall/61430-medline-recalls-curad-reusable-gel-hot-cold-packs-for-latex · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0633-2022
Cite this page
“Medline Recalls CURAD Reusable Gel Hot/Cold Packs for Latex Mislabeling.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61430-medline-recalls-curad-reusable-gel-hot-cold-packs-for-latex. Based on FDA recall #Z-0633-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0633-2022%22&limit=1).
Why it’s dangerous
The product contains natural rubber latex but is labeled as latex-free. This mislabeling could cause allergic reactions in people sensitive to latex, especially if the product is used frequently.
Who’s affected
People who own or use CURAD reusable gel hot/cold packs with the listed item numbers are affected. Those with latex allergies are at higher risk.
How to tell if you have this one
Check the product label for item numbers starting with CUR959 or TGT0114V1. The specific lot numbers listed in the recall are also on the product.
- Brand
Medline- Category
Medical device
What to do — step by step
Check Product Label
Look for item numbers listed in the recall (CUR959/CUR959H or TGT0114V1) on the product.
How this recall unfolded
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest medical device recalls
Keep exploring
Where this comes from
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-0633-2022 (December 15, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0633-2022 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.