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Ultra Seal Corporation

Ultra Seal Corporation Recalls

All product recalls associated with Ultra Seal Corporation.

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Recall Summary

Total Recalls

814

Past Year

Class I (Serious)

186

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 241–260 of 814 recalls

Advance Pain Reliever (Ultra Seal) – Stability Failure (2021)

Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.

Class IIILow

FDAOct 13, 2021Nationwide• Ultra Seal Corporation

Pain Free Plus X-Strength (Ultra Seal) – Stability Failure (2021)

Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.

Class IIILow

FDAOct 13, 2021Nationwide• Ultra Seal Corporation

Xpect First Aid Pain Away (Ultra Seal) – Stability Specification Failure (2021)

Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.

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Class III

Low

FDAOct 13, 2021Nationwide• Ultra Seal Corporation

PainAway II (Ultra Seal) – Stability Specification Failure (2021)

Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.

Class IIILow

FDAOct 13, 2021Nationwide• Ultra Seal Corporation

AERO Tab Pain Reliever (Ultra Seal) – Stability Specification Failure (2021)

Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.

Class IIILow

FDAOct 13, 2021Nationwide• Ultra Seal Corporation

ZEE+ Painaid ESF (Ultra Seal) – Stability Specification Failure (2021)

Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.

Class IIILow

FDAOct 13, 2021Nationwide• Ultra Seal Corporation

Seafood Products (Northeast Seafood) – Salmonella contamination (2021)

Salmonella

Seafood and fin fish products potentially contaminated with Salmonella and implicated in illness outbreak

Class IHigh

FDAOct 7, 2021CO, IN• Northeast Seafood Products, Incorporated

Oceanic Adult Dry Top Snorkels (Unique Sea) – drowning risk (2021)

This recall involves Oceanic Adult Dry Top Snorkels. The recalled snorkels are white and gray with a blue plastic housing around an oval shaped, clear rubber bottom purge valve and a blue dry splash guard located at the top of the snorkel. The snorkel measures about 16.5 inches tall. Oceanic Adult Dry Top Snorkels with the following four-digit batch numbers are included in this recall: 2038, 2039, 2040, 2041, 2042, 2043, 2044, 2045, 2046, 2047, 2048, 2049, 2050, 2051, 2102, 2103, 2104, 2105, 2106, 2107, 2108, 2109, 2110, 2111, 2112, 2113, 2114 and 2115. The batch numbers can be found above the flexible gray tubing.

CPSCSep 22, 2021Nationwide• Unique Sea Products, of Thailand

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation/RayPlan versions 4 - 11A, including service pa...

An issue where the combined density in a dose grid voxel partially covered by the External ROI and also partially covered by an ROI of type Bolus, Support or Fixation may be unexpected.The density in the voxel can be both under- and overestimated

FDASep 22, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: TomoHelical and TomoDirect plans in RayStation 6, 7, 8A, ...

If the dynamic jaw mode is used and an optimization is continued after changing the dose grid or modifying the target ROI, the positions of the jaws may change unexpectedly for some control points. User must be aware to avoid unnecessary jaw openings during treatment planning

FDASep 9, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Banquet Cut Salmon (Seabear) – Botulinum Risk (2021)

Potential for growth of C. botulinum

Class IIModerate

FDASep 8, 2021AZ, CA, GA +1 more• Seabear Company

Versea Diagnostics LLC: Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood...

Products may have been distributed to customers other than laboratories certified under the Clinical Laboratory Improvement Amendments as stipulated in the Emergency Use Authorization.

FDAJul 27, 2021Nationwide• Versea Diagnostics LLC

Versea Diagnostics LLC: CareStart COVID-19 Antigen Rapid Diagnostic Test for the ...

Products may have been distributed to customers other than laboratories certified under the Clinical Laboratory Improvement Amendments as stipulated in the Emergency Use Authorization.

FDAJul 27, 2021Nationwide• Versea Diagnostics LLC

Versea Diagnostics LLC: Status COVID-19/Flu Rapid Immunoassay for Direct Detectio...

Products may have been distributed to customers other than laboratories certified under the Clinical Laboratory Improvement Amendments as stipulated in the Emergency Use Authorization.

FDAJul 27, 2021Nationwide• Versea Diagnostics LLC

Versea Diagnostics LLC: FaStep COVID-19 IgG/IgM Rapid Test Device Qualitative de...

Products may have been distributed to customers other than laboratories certified under the Clinical Laboratory Improvement Amendments as stipulated in the Emergency Use Authorization.

FDAJul 27, 2021Nationwide• Versea Diagnostics LLC

Chicken of the Sea Genova Meal Kit (Chicken of the Sea) – Quality Concerns (2021)

Promotional Genova Meal Kits included products prepared in home kitchen that did not meet quality standards.

Class IIModerate

FDAJun 30, 2021CA, FL, GA +9 more• Chicken of the Sea; Thai Union

SEALIGHT LED HEADLIGHT BULB Equipment Recall: EXTERIOR LIGHTING:HEADLIGHTS:BULBS

Shenzen YouCheng Dianzishangwu Youxiangg (Sealight) is recalling certain Sealight S1H11 LED headlight bulbs with part number AHDS1H11-E. These bulbs can create excessive glare or brightness to oncoming traffic. As such, these bulbs fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

NHTSAJun 17, 2021Nationwide• SEALIGHT

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation (Radiation Treatment Planning System) : RaySta...

Initial delivery positions will be set incorrectly when having setup beam(s) at the localization point.

FDAJun 8, 2021TN• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

2021 SEA-DOO MOVE I EXTENDED 1500 Recall: WHEELS

Bombardier Recreation Products, Inc. (BRP) is recalling certain 2021 Sea-Doo Move I Extended 1500 trailers. The wheel spindles were improperly welded to the axle.

NHTSAJun 3, 2021Nationwide• SEA-DOO

2020 SEAGRAVE MARAUDER Recall: FUEL SYSTEM, DIESEL:FUEL INJECTION SYSTEM:FUEL RAIL

Fire/Burn Risk

Seagrave Fire Apparatus, LLC (Seagrave) is recalling certain 2017-2020 Marauder, Attacker and Capitol vehicles. The sealing washer may not seat correctly in the pilot bore holes, allowing the high pressure fuel rail assembly to leak.

NHTSAMay 25, 2021Nationwide• SEAGRAVE