Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 2 LINE (10) Model/Catalog Number: DT-7044-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No
Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 2 LINE (10) Model/Catalog Number: DT-7044-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No was recalled because due to incorrect expiration date on product manufactured between september 2016 to march 2023. products are labeled with a 10 year shelf life. the correct validated shelf life is 5 years.. If you have this product, stop using it until you verify your lot or model details.
By RecallRadar Editorial Team
Sourced from FDA. Last verified October 13, 2026.
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Check if you qualifyKey facts
- Date announced
- October 7, 2026
- Source agency
- FDA
This recall involves safety concerns. Take action promptly.
✨ Plain-English Summary
Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 2 LINE (10) Model/Catalog Number: DT-7044-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No was recalled because due to incorrect expiration date on product manufactured between september 2016 to march 2023. products are labeled with a 10 year shelf life. the correct validated shelf life is 5 years.. If you have this product, stop using it until you verify your lot or model details.
Is This Recall Still Active?
Status: Yes - Active
This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.
What's Being Recalled
Quoted source excerpt from the official notice.
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
Quick Info
Key facts from the official notice, kept in the article flow for easy cross-checking.
- Brand
- Asp global, llc.
- Category
- medical
- Source agency
- FDA
- Announced
- October 7, 2026
- Country
- US
- Status
- Active
Who's Affected
Specific models and identifiers listed in the source notice:
Model #1
Lot Code: Model Number: DT-7044-02Q UDI-DI: UDI (01) 00840001403253 All Lots produced from 01SEP2016 to 01MAR2023: S0823STY, R1201STY, N0330STY, N0530STY, M0730STY, M0930STY
| # | Model |
|---|---|
| 1 | Lot Code: Model Number: DT-7044-02Q UDI-DI: UDI (01) 00840001403253 All Lots produced from 01SEP2016 to 01MAR2023: S0823STY, R1201STY, N0330STY, N0530STY, M0730STY, M0930STY |
Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.
What You Should Do
Follow the remedy path from the official notice using the exact model and serial details above.
- 1Stop using the affected product until you verify whether your item is impacted.
- 2Check the official recall notice and match your model, lot, or serial details.
- 3Follow the official instructions for repair, replacement, refund, or disposal.
Source & Verification
This page summarizes the official notice and keeps key facts easy to verify.
- Official source
- FDA
- Announced by source
- October 7, 2026
- Last reviewed by RecallRadar
- October 13, 2026
Frequently Asked Questions
Am I affected by this recall?
Check the affected models section on this page. The official notice currently lists Lot Code: Model Number: DT-7044-02Q UDI-DI: UDI (01) 00840001403253 All Lots produced from 01SEP2016 to 01MAR2023: S0823STY, R1201STY, N0330STY, N0530STY, M0730STY, M0930STY.
What is the remedy for this recall?
Follow the official instructions for repair, replacement, refund, or disposal on the asp global, llc. recall page.
Where can I verify recall details?
Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/device/enforcement.json?search=recall_number:Z-0060-2027&limit=1
Keep browsing with these internal hubs: asp global, llc. recall hub and Medical recall hub.
Official Resources
Use these primary sources for final eligibility and claim instructions.
View official notice from FDASee an inaccuracy?
Help us improve the accuracy of this recall information.
On this page
Free checker
Check if you qualify
See whether your device may qualify for a free repair or replacement program before you spend money.
Check if you qualifyKey facts
- Date announced
- October 7, 2026
- Source agency
- FDA
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