Severity
Moderate
ModerateActive
CPSC recall · Reported March 7, 2013
U.S. Divers Recalls Youth Snorkeling Mask Sets Due to Laceration Hazard; Sold Exclusively at Costco
Notches in the tempered glass lens on the mask can break under certain water pressure, posing a laceration hazard to the user.
Aqua Lung Inc., of Vista, Calif. recalled This recall involves Martinique Jr. single paned, tempered glass youth snorkeling masks s… — a moderate-severity action.
U.S. Divers Recalls Youth Snorkeling Mask Sets Due to Laceration Hazard; Sold Exclusively… was recalled by Aqua Lung Inc., of Vista, Calif. in March 7, 2013. Reason: Notches in the tempered glass lens on the mask can break under certain water pressure, posing a laceration ha…. Remedy: Consumers should immediately stop using the recalled masks and contact U.S. Divers for a …. Verify recall #13133 with the CPSC before acting.
The recall
Aqua Lung Inc., of Vista, Calif. issued this moderate-severity CPSC recall — Notches in the tempered glass lens on the mask can break under certain water pressure, posing a laceration ha….
- Moderate
- severity level
- March 7, 2013
- reported
Sourced from official CPSC enforcement records. Verify recall #13133 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #13133) was formally reported on March 7, 2013. It is classified under Moderate severity, with a current status of Active. Aqua Lung Inc., of Vista, Calif. is listed as the recalling firm. Federal records list the affected scope as About 44,000 units.
The documented reason for this recall is: Notches in the tempered glass lens on the mask can break under certain water pressure, posing a laceration hazard to the user. 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 recalled masks and contact U.S. Divers for a replacement mask. — 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 — 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.
Household Products recalls over time
Where this recall sits in its category — 2,542 household products recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 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 44,000 units
Related Recalls
6
0 from same agency
Product description
This recall involves Martinique Jr. single paned, tempered glass youth snorkeling masks sold in a set with snorkel and fins. The masks feature a silicone face skirt, strap and adjustable buckles. The mask is blue with a silver accent piece that frames the tempered glass lens. The U.S. Divers logo is on the upper bridge of the mask as well as inset on the tempered glass lens. The lens is also labeled as tempered. The buckles are each printed with the U.S. Divers "wave" logo.
Reason for recall
Notches in the tempered glass lens on the mask can break under certain water pressure, posing a laceration hazard to the user.
Remedy — what to do
Consumers should immediately stop using the recalled masks and contact U.S. Divers for a replacement mask.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 13133 |
| Date reported | March 7, 2013 |
| Date initiated | March 7, 2013 |
| Recalling firm | Aqua Lung Inc., of Vista, Calif. |
| Affected scope | About 44,000 units |
| 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 recalled masks and contact U.S. Divers for a replacement mask.
- Check the recall number (13133) 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? ▼
This recall involves Martinique Jr. single paned, tempered glass youth snorkeling masks sold in a set with snorkel and fins. The masks feature a silicone face skirt, strap and adjustable buckles. The mask is blue with a silver accent piece that frames the tempered glass lens. The U.S. Divers logo is on the upper bridge of the mask as well as inset on the tempered glass lens. The lens is also labeled as tempered. The buckles are each printed with the U.S. Divers "wave" logo.. Recalled by Aqua Lung Inc., of Vista, Calif.. Units affected: About 44,000 units.
Why was this product recalled? ▼
Notches in the tempered glass lens on the mask can break under certain water pressure, posing a laceration hazard to the user.
What should consumers do? ▼
Consumers should immediately stop using the recalled masks and contact U.S. Divers for a replacement mask.
Which agency issued this recall? ▼
This recall was issued by the CPSC on March 7, 2013. Severity: Moderate. Recall number: 13133.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (13133) 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.
Continue exploring
Keep tracking product safety across the federal recall archive.
Recall Checker
Search the full archive by product name, brand, or recall number across every agency.
Check a product →
CPSC recalls
Every recall issued by CPSC, newest first.
Browse the feed →
RecallRadar
Live feed of the latest recalls across the FDA, CPSC and NHTSA — filter by agency and severity.
View the live feed →
Rankings
The largest recalls by units affected and the most-recalled product categories.
See the rankings →
Browse by category
Find recalls by product type to spot recurring defect patterns.
All categories →
What to do next
A step-by-step guide to refunds, repairs, and returns after a recall.
Read the guide →
Nearby Recalls in This Category
Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
FDA Food Moderate
Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed 8 bags per master case of 2 Kg (4.41 lb) each total case wei…
Disaronno Ingredients S.p.a. · 2026-05-13
FDA Drug Moderate
Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054,…
Wells Pharma of Houston LLC · 2026-05-06
FDA Drug Moderate
fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, ND…
Wells Pharma of Houston LLC · 2026-05-06
FDA Drug Moderate
fentaNYL Citrate injectable Solution in 0.9% Sodium Chloride, Narcotic, (2500 mcg/ 250 mL) (10 mcg per mL), 250 mL bag,…
Wells Pharma of Houston LLC · 2026-05-06
FDA Drug Moderate
fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houst…
Wells Pharma of Houston LLC · 2026-05-06
Compare this recall with Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed … →
Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported March 7, 2013.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.