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Fish Recalls in the United States

9350 food recalls involving fish tracked from FDA open data. Updated daily.

9350 Fish Recalls

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medical Class II
2026-04-22

Linkbio Corp. recalls LinkBio CORE Workstation, a component of the CORE Shoulder S

The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

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medical Class II
2026-04-22

Beta Bionics, Inc. recalls iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software

it was found that in versions 1.3.7, 1.4.2, and 1.4.3, the Lock Screen and Limited Access Passcode Screen on the iLet graphical user interface (GUI) include certain icons displayed in the status bar that are active, thereby allowing the user to bypass those screens when those icons on the status bar are pressed, allowing unauthorized access while the device is in Limited Access Mode. A Health Risk associated with Limited access mode includes severe hypoglycemia due to unauthorized access to the iLet if someone were to make unauthorized meal announcements or stopped insulin delivery.

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Food Class I
2026-04-15

AYCO FARMS INC recalls Fresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped in

Potential Salmonella Contamination

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Food Class II
2026-04-22

Booey's Gourmet LLC recalls Booey's Dragon's Breath sauce, 15.2oz ringneck glass bottle.

Ingredients statement declares Anchovy and Sasame, but Contains statement does not declare Fish (Anchovy) and Sesame.

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medical Class II
2026-04-15

Beckman Coulter, Inc. recalls MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI c

Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.

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Food Class I
2026-04-15

Pure Vitamins and Natural Supplements, LLC recalls Red Bull Extreme Male Enhancement Supplement, total of 15 po

FDA analysis revealed the presence of undeclared sildenafil

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Food Class I
2026-04-15

Pure Vitamins and Natural Supplements, LLC recalls Blue Bull Extreme Male Enhancement Supplement, total of 15 p

FDA analysis revealed the presence of undeclared sildenafil

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Food Class II
2026-04-15

Riverence Provisions LLC recalls Riverence Smoked Trout Dip, net wt. 7oz. Product is perishab

Label declares cream cheese but does not declare milk

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medical Class I
2026-03-18

Trividia Health, Inc. recalls Owner's Booklets and Instructions for Use that are used with

The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.

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medical Class II
2026-03-18

Covidien LLC recalls HealthCast "Vital Sync" Remote Patient Monitoring System whi

Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient monitoring system.

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medical Class I
2026-03-18

Trividia Health, Inc. recalls Owner's Booklets and Instructions for Use that are used with

The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.

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medical Class II
2026-03-18

Physio-Control, Inc. recalls PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Ele

Due to pediatric defibrillator electrode delamination

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medical Class II
2026-03-18

Raz Design Inc recalls Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog

Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place.

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medical Class I
2026-03-18

Trividia Health, Inc. recalls Owner's Booklets and Instructions for Use that are used with

The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.

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medical Class I
2026-03-18

Trividia Health, Inc. recalls Owner's Booklets and Instructions for Use that are used with

The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.

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medical Class II
2026-03-25

Baxter Healthcare Corporation recalls Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spo

Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.

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medical Class II
2026-04-01

Beckman Coulter, Inc. recalls MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212

Due to the likely presence of contamination in well(s).

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medical Class II
2026-04-08

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

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medical Class II
2026-04-08

Cardinal Health 200, LLC recalls Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock,

The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages are U-100 Insulin syringes.

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medical Class II
2026-04-08

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

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