Severity
Moderate
Scuba Diving Buoyancy Compensators Recalled by Ocean Management Systems Due to Drowning Hazard
Reported: April 28, 2010 Initiated: April 28, 2010 #10208 About 20,000 units
Ocean Management Systems Inc., of Middletown, N.Y. issued this CPSC recall on April 28, 2010. Classified as Moderate severity. Approximately About 20,000 units are affected. The recall was issued because: The buoyancy compensator seal ring could crack, posing a drowning hazard to divers.. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
Recall Insight
This CPSC action (record #10208) was formally reported on April 28, 2010. It is classified under Moderate severity, with a current status of Active. Ocean Management Systems Inc., of Middletown, N.Y. is listed as the recalling firm. Federal records indicate About 20,000 units are affected.
The documented reason for this recall is: The buoyancy compensator seal ring could crack, posing a drowning hazard to divers. 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 diving equipment and contact Ocean Management Systems to receive a free repair. — consumers holding this product should act on that instruction rather than relying on general guidance.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 16 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Recall Distribution by Severity Class
Units Affected
About 20,000
Related Recalls
6
0 from same agency
Product Description
This recall involves buoyancy compensators with the following model numbers. Buoyancy compensators provide buoyancy control for scuba divers by allowing them to inflate or deflate the devices. The compensators were sold in black or red. "OMS" is printed on the front inside of the compensators. Item and serial numbers are printed on the warning label located in the non-inflation area of the buoyancy compensator. A list of serial numbers included in this recall is available from the firm. Item Number Description BC-TCPS- B TACOPS® BC ; Black BC-TCPS-R TACOPS® BC ; Red BC116-32B16 B Non retraction single tank BC 32 lb. lift / Black BC116-32R Non retraction single tank BC 32 lb. lift / Red BC-LGS45 Larry Green Signature Series 45 lb. lift BC BC-LGS70 Larry Green Signature Series 70 lb. lift BC BC118 - K Dual Bladder BC [inflated] 94 lb. lift Black or Red BC115 - KB Dual Bladder BC, 60 lb. lift in Black BC115 - KR Dual Bladder BC, 60 lb. lift in Red BC118 - K Dual Bladder BC [deflated] 94 lb. lift Black or Red BC117 - K45 Single Bladder BC 45 lb. lift / Black BC117CR - K45 Chemically Resistant 45 lb. lift / Black BC117 - K60 Single Bladder BC, 60 lb. lift / Black BC117 - KB Single Bladder BC, 94 lb. lift / Black BC117 - KR Single Bladder BC, 94 lb. lift / Red BC116-45B Non-retraction Single Bladder BC 45 lb. lift/ Black BC116-60B Non-retraction Single Bladder BC 60 lb. lift/ Black BC116-60R Non-retraction Single Bladder BC 60 lb. lift/ Red BC116-60C Chemically Resistant 60 lb. lift / Black
Reason for Recall
The buoyancy compensator seal ring could crack, posing a drowning hazard to divers.
Remedy
Consumers should immediately stop using the diving equipment and contact Ocean Management Systems to receive a free repair.
Details
- Recalling Firm
- Ocean Management Systems Inc., of Middletown, N.Y.
- Units Affected
- About 20,000
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 10208 |
| Date reported | April 28, 2010 |
| Date initiated | April 28, 2010 |
| Recalling firm | Ocean Management Systems Inc., of Middletown, N.Y. |
| Units affected | About 20,000 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
Frequently Asked Questions
What product was recalled? ▼
This recall involves buoyancy compensators with the following model numbers. Buoyancy compensators provide buoyancy control for scuba divers by allowing them to inflate or deflate the devices. The compensators were sold in black or red. "OMS" is printed on the front inside of the compensators. Item and serial numbers are printed on the warning label located in the non-inflation area of the buoyancy compensator. A list of serial numbers included in this recall is available from the firm. Item Number Description BC-TCPS- B TACOPS® BC ; Black BC-TCPS-R TACOPS® BC ; Red BC116-32B16 B Non retraction single tank BC 32 lb. lift / Black BC116-32R Non retraction single tank BC 32 lb. lift / Red BC-LGS45 Larry Green Signature Series 45 lb. lift BC BC-LGS70 Larry Green Signature Series 70 lb. lift BC BC118 - K Dual Bladder BC [inflated] 94 lb. lift Black or Red BC115 - KB Dual Bladder BC, 60 lb. lift in Black BC115 - KR Dual Bladder BC, 60 lb. lift in Red BC118 - K Dual Bladder BC [deflated] 94 lb. lift Black or Red BC117 - K45 Single Bladder BC 45 lb. lift / Black BC117CR - K45 Chemically Resistant 45 lb. lift / Black BC117 - K60 Single Bladder BC, 60 lb. lift / Black BC117 - KB Single Bladder BC, 94 lb. lift / Black BC117 - KR Single Bladder BC, 94 lb. lift / Red BC116-45B Non-retraction Single Bladder BC 45 lb. lift/ Black BC116-60B Non-retraction Single Bladder BC 60 lb. lift/ Black BC116-60R Non-retraction Single Bladder BC 60 lb. lift/ Red BC116-60C Chemically Resistant 60 lb. lift / Black. Recalled by Ocean Management Systems Inc., of Middletown, N.Y.. Units affected: About 20,000.
Why was this product recalled? ▼
The buoyancy compensator seal ring could crack, posing a drowning hazard to divers.
What should consumers do? ▼
Consumers should immediately stop using the diving equipment and contact Ocean Management Systems to receive a free repair.
Which agency issued this recall? ▼
This recall was issued by the CPSC on April 28, 2010. Severity: Moderate. Recall number: 10208.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (10208) 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.
Recall Guides
Learn how the US recall system works and how to protect yourself and your household.
How the US Recall System Works
The three federal agencies, how recalls are initiated, and what happens next.
Understanding Recall Severity Classes
What Class I, II, and III mean and which recalls demand immediate action.
What to Do When a Product Is Recalled
Verify, claim your remedy, report injuries, and navigate the process.
How to Check If Your Products Are Recalled
Step-by-step guide to checking food, products, medications, and vehicles.
Recalled Products in Your Home
A room-by-room household audit guide for active recalls.
Most Recalled Product Categories
Rankings of highest-recall categories from FDA, CPSC, and NHTSA.
Recall Context
Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
Related Safety Data
Explore related product safety and public health data from federal sources.
Food Safety Inspections
FDA and state food facility inspection results — violations, enforcement actions, and compliance history for food manufacturers and processors.
PlainFoodSafe →
Ingredient Safety Data
FDA food additive and ingredient safety database — regulatory status, usage limits, and safety assessments for thousands of ingredients.
PlainIngredients →
Nutrition Data
USDA nutrition facts for 2M+ food items — calories, macros, vitamins, and ingredient analysis to verify what you consume.
GetFoodFacts →
Drug Safety Information
FDA drug data for 680+ medications — interactions, alternatives, side effects, and safety information for recalled and active drugs.
PlainMeds →
Product Injury Data
CPSC emergency room injury data for 838 product categories — 7.3M NEISS records tracking real-world consumer product injuries.
PlainSafety →
Recall Checker
Search our database of 83K+ recalls by product name, brand, or recall number across all agencies.
Check Now →
Recall Radar
Live feed of the latest recalls across FDA, CPSC, NHTSA, and USDA — filter by agency and severity.
View Radar →
Nearby Recalls in This Category
Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
FDA Devices Moderate
Endo-Model Replacement Plateau; Item Number: 15-0027/11;
Waldemar Link GmbH & Co. KG (Mfg Site) · 2026-03-18
FDA Devices Low
Penner Pacific Bathing Spa, Model Numbers 360020-1P
Penner Patient Care, Inc. · 2026-03-18
FDA Devices Moderate
GEM Premier 5000 PAK, Part No. 00055360004.
Instrumentation Laboratory · 2026-03-18
FDA Devices Moderate
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
Beckman Coulter Mishima K.K. · 2026-03-18
FDA Devices Critical
Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Descript…
Trividia Health, Inc. · 2026-03-18
Compare this recall with Endo-Model Replacement Plateau; Item Number: 15-0027/11; →
Data Sources
Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
- 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)
- Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product 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.
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- U.S. Census Bureau ACS — demographic + housing + income data. census.gov/programs-surveys/acs
- BLS Occupational Employment and Wage Statistics (OEWS) — wage + employment by occupation. bls.gov/oes
- BEA Regional Economic Accounts — GDP + personal income by state/metro. bea.gov/data/regional
- U.S. Census Bureau County Business Patterns — establishment + employment by industry. census.gov/cbp
- IRS Statistics of Income (SOI) — tax-return aggregate data. irs.gov/statistics
- data.gov — U.S. federal open-data portal — discovery layer for additional federal sources. data.gov
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).