Severity
Moderate
ModerateActive
CPSC recall · Reported April 19, 2012
XS Scuba Recalls Miflex High Pressure Diving Hoses Due to Drowning Hazard
The diving hose can rupture reducing the available air supply to the diver, posing a drowning hazard.
Miflex 2, Villasanta, Italy recalled The high pressure hose is used to monitor cylinder pressure for the air supply in tanks f… - a moderate-severity action.
XS Scuba Recalls Miflex High Pressure Diving Hoses Due to Drowning Hazard was recalled by Miflex 2, Villasanta, Italy in April 19, 2012. Reason: The diving hose can rupture reducing the available air supply to the diver, posing a drowning hazard.. Remedy: Consumers should immediately stop using the hoses and contact XS Scuba to receive instruc…. Verify recall #12155 with the CPSC before acting.
The recall
Miflex 2, Villasanta, Italy issued this moderate-severity CPSC recall-The diving hose can rupture reducing the available air supply to the diver, posing a drowning hazard..
- Moderate
- severity level
- April 19, 2012
- reported
Sourced from official CPSC enforcement records. Verify recall #12155 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #12155) was formally reported on April 19, 2012. It is classified under Moderate severity, with a current status of Active. Miflex 2, Villasanta, Italy is listed as the recalling firm. Federal records list the affected scope as About 17,000.
The documented reason for this recall is: The diving hose can rupture reducing the available air supply to the diver, posing a drowning hazard. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately stop using the hoses and contact XS Scuba to receive instructions for obtaining a free replacement hose. - consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls, 3 from CPSC - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
About 17,000
Related Recalls
6
3 from same agency
Product description
The high pressure hose is used to monitor cylinder pressure for the air supply in tanks for scuba diving. The hoses have MFX stamped on the hose's end fitting. They were sold as individual replacement gauge hoses and as cascade hoses and in the following kits and model numbers: Deluxe Cylinder Equalizer w/ Miflex HP hose P/N AC366 Miflex Two-Gauge Console HL300/HL300M Miflex Rebreather Kits MRB-EVO-LG, MRB-EVO-MD & MRB-ISP-POST-LG
Reason for recall
The diving hose can rupture reducing the available air supply to the diver, posing a drowning hazard.
Remedy, what to do
Consumers should immediately stop using the hoses and contact XS Scuba to receive instructions for obtaining a free replacement hose.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 12155 |
| Date reported | April 19, 2012 |
| Date initiated | April 19, 2012 |
| Recalling firm | Miflex 2, Villasanta, Italy |
| Affected scope | About 17,000 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately stop using the hoses and contact XS Scuba to receive instructions for obtaining a free replacement h…
- Check the recall number (12155) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
The high pressure hose is used to monitor cylinder pressure for the air supply in tanks for scuba diving. The hoses have MFX stamped on the hose's end fitting. They were sold as individual replacement gauge hoses and as cascade hoses and in the following kits and model numbers: Deluxe Cylinder Equalizer w/ Miflex HP hose P/N AC366 Miflex Two-Gauge Console HL300/HL300M Miflex Rebreather Kits MRB-EVO-LG, MRB-EVO-MD & MRB-ISP-POST-LG. Recalled by Miflex 2, Villasanta, Italy. Units affected: About 17,000.
Why was this product recalled? ▼
The diving hose can rupture reducing the available air supply to the diver, posing a drowning hazard.
What should consumers do? ▼
Consumers should immediately stop using the hoses and contact XS Scuba to receive instructions for obtaining a free replacement hose.
Which agency issued this recall? ▼
This recall was issued by the CPSC on April 19, 2012. Severity: Moderate. Recall number: 12155.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (12155) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
CPSC Moderate
Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Serious Injury from Fire and Burn Hazards
· 2026-07-02
CPSC Moderate
Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Heat Pumps Due to Risk of Serious Injury f…
· 2026-06-25
CPSC Moderate
Arizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by…
· 2026-06-18
FDA Devices Moderate
GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used i…
GE Medical Systems Information Technologies Inc · 2026-06-03
FDA Devices Critical
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit…
Medline Industries, LP · 2026-06-03
Compare this recall with Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Ser… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: CPSC, reported April 19, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.