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Stanley Pearlman Enterprises, Inc.

Stanley Pearlman Enterprises, Inc. Recalls

All product recalls associated with Stanley Pearlman Enterprises, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

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 781–800 of 37661 recalls

Whiting Fillet (Stanley Pearlman) – incorrect date labeling (2025)

Recall initiated due to the wrong best by date (1-11-2025) being printed on the retail bag which would imply that these are expired but in truth they are good until 1-11-2027.

Class IIILow

FDAAug 15, 2025MD, PA• Stanley Pearlman Enterprises, Inc.

Breaded Shrimp (AquaStar) – Cesium-137 contamination (2025)

Product may be contaminated with Cesium-137 (Cs-137).

Class IIModerate

FDAAug 14, 2025AL, AK, AR +27 more• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Altec Digger Derrick (Altec) – Winch Bumper Fastener Issue (2025)

Altec Industries, Inc. (Altec) is recalling certain 2024-2025 Aerial Device, and Digger Derrick vehicles. The front winch bumper may be secured with incorrect bolts, which can cause the bumper to detach from the vehicle.

1...38 394041 42...1884

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High

NHTSAAug 14, 2025Nationwide• ALTEC

Jayco Jay Flight SLX (Jayco) – Missing Furnace Vent (2025)

Jayco, Inc. (Jayco) is recalling certain 2024-2025 Jay Flight SLX travel trailers. The furnace exhaust vent may be missing from the exterior wall, allowing carbon monoxide to enter the vehicle.

Very High

NHTSAAug 14, 2025Nationwide• JAYCO TRAVEL TRAILER

Kroger Cooked Shrimp (AquaStar) – Cesium-137 contamination (2025)

Product may be contaminated with Cesium-137 (Cs-137).

Class IIModerate

FDAAug 14, 2025AL, AK, AR +27 more• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

AquaStar Cocktail Shrimp (Admiralty Island) – Cesium-137 contamination (2025)

Product may be contaminated with Cesium-137 (Cs-137).

Class IIModerate

FDAAug 14, 2025AL, AK, AR +27 more• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

UniCel DxH 900 Analyzer (Beckman Coulter) – Hemoglobin Result Error (2025)

Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.

Moderate

FDAAug 13, 2025Nationwide• Beckman Coulter Inc.

UniCel DxH 690T Analyzer (Beckman Coulter) – Hemoglobin Result Error (2025)

Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.

Moderate

FDAAug 13, 2025Nationwide• Beckman Coulter Inc.

UniCel DxH 600 Analyzer (Beckman Coulter) – Hemoglobin Result Error (2025)

Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.

Moderate

FDAAug 13, 2025Nationwide• Beckman Coulter Inc.

Philips CT System (Philips) – Patient Table Descent Risk (2025)

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Moderate

FDAAug 13, 2025Nationwide• Philips North America Llc

UniCel DxH 800 Analyzer (Beckman Coulter) – Hemoglobin Result Error (2025)

Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.

Moderate

FDAAug 13, 2025Nationwide• Beckman Coulter Inc.

Change Healthcare Radiology Software (Change Healthcare) – Report Display Issue (2025)

Due to software issue, radiology reports may not be fully displayed when viewing.

Low

FDAAug 13, 2025Nationwide• CHANGE HEALTHCARE CANADA COMPANY

NutraGlide Nasal Feeding Tube (Applied Medical) – Tip Detachment Risk (2025)

The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

High

FDAAug 12, 2025MA, RI• Applied Medical Technology Inc

Quesito Colombian Cheese (El Establo) – Listeria risk (2025)

Listeria

Product was manufactured and held under insanitary conditions. Product may be contaminated with Listeria monocytogenes.

Class IHigh

FDAAug 12, 2025MA• Quesito El Establo

FLEX Monoclonal Mouse Antibody (Agilent) – weak staining (2025)

Their is the potential for weak staining which may result in false negative CD20 identification.

Moderate

FDAAug 11, 2025Nationwide• Agilent Technologies Denmark ApS 42 PRODUKTIONSVEJ Glostrup Denmark

Atellica CH Protein Test (Siemens) – false result risk (2025)

Potential for falsely depressed patient, quality control (QC), and/or calibration results or delayed results.

Low

FDAAug 11, 2025Nationwide• Siemens Healthcare Diagnostics, Inc.

Merge Hemo Software (Merge Healthcare) – patient data issue (2025)

Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an issue with the Schiller ARGUS PB-3000 Patient Data Module (PDM) where certain units trigger an error message on the Merge Hemo Client (Pressure Sensor Defective) during non-invasive blood pressure (NIBP) measurements, specifically when the initial inflation pressure is set in the high-pressure range (>240 mmHg). The ARGUS PB-3000 is a vital signs monitoring instrument intended to be integrated into the Merge Hemo System. No other components of the Merge Hemo System are affected.

Moderate

FDAAug 11, 2025Nationwide• Merge Healthcare, Inc.

VACUETTE Coagulation Tube (Greiner) – label misplacement (2025)

Blood collection tubes were manufactured with the label applied too high on the tube, which shifted the printed fill level mark upward, which could result in unnecessary sample rejection and repeat collections.

Low

FDAAug 8, 2025Nationwide• Greiner Bio-One North America, Inc.

RayStation Software (RaySearch) – UID uniqueness (2025)

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Low

FDAAug 8, 2025Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Argus PB-3000 Monitor (Schiller) – measurement error (2025)

Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.

Moderate

FDAAug 8, 2025Nationwide• Schiller, Ag Altgasse 68 Baar Switzerland