Allergen Hub
Fish Recalls in the United States
9728 food recalls involving fish tracked from FDA open data. Updated daily.
9728 Fish Recalls
All food recalls →Ethicon, LLC recalls PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical
Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that if discovered prior to use may cause surgical delay. If used, fluid could cause reduced suture tensile strength or knot security, tissue irritation/inflammatory tissue response, and treatment failure, including wound dehiscence/bleeding.
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Cadwell Industries Inc recalls Brand Name: IOMAX Product Name: IOMAX Cortical Module Mode
Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the patient, or allow an unintended electrical current to reach the patient.
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Baxter Healthcare Corporation recalls Likorall Overhead Lifts Product Code: 3121001 Product De
Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap lowers more quickly than expected during use. Patients are at some risk for injury if a significant fall/drop were to occur due to this issue.
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Stewart's Shops Corp. recalls Stewarts Shops Vanilla Heavenly Medley 1/2 Gallon (1.89 L),
Foreign object: May contain pieces of metal
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K.C. Pharmaceuticals, Inc. recalls Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ (15 mL
Lack of Assurance of Sterility
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Berlin Seeds recalls Berlin Seeds Alfalfa Sprouting Seeds, packaged in 1/4 lb., 1
Product contains alfalfa seed recalled by the supplier due to potential E. coli and/or Salmonella contamination.
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Karl Storz Endoscopy recalls HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 0404855
Due to incorrect inside packaging label for eyepiece.
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Alere San Diego, Inc. recalls Fisher Scientific Sure-Vue Urine hCG Strip, Model/ Part: FHC
hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.
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HeartSine Technologies Ltd recalls HeartSine samaritan PAD (Public Access Defibrillator); Hea
Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check.
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Alere San Diego, Inc. recalls McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5
hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.
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Beckman Coulter Mishima K.K. recalls Systems/units containing affected software/SQL BECKMAN COUL
Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may output the message System Stopped By Fatal Error: DBConnectionError AlarmDB when launching the instrument software, using PC pre-installed with Microsoft SQL Server 2022 Express. When this occurs, AlarmDB becomes unreadable and the instrument software cannot be started. This causes a delay in obtaining patient results.
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Alere San Diego, Inc. recalls Fisher Scientific Sure-Vue Urine hCG, Model/ Part: FHC-102/2
hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.
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Bard Peripheral Vascular Inc recalls EnCor EnCompass Breast Biopsy and Tissue Removal System Cons
Breast biopsy and tissue removal system may experience the following errors: 1) Probe calibration and /or handheld driver failure (code HH01-00020009) , 2) Pressure sensor (code E01-0054000E), which prompts the user to restart and re-calibrate; errors may lead to interruption or prolongation of the biopsy procedure, or the need for additional tissue sampling or repeat biopsy.
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Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology REF
Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter.
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Alere San Diego, Inc. recalls Fisher Scientific Sure-Vue Serum/Urine hCG, Model/ Part: FHC
hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.
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Philips North America Llc recalls Philips Medical Systems Technologies Ltd. Spectral CT 7500,
The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in the patient receiving additional radiation.
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TODD'S SEEDS LLC recalls Todd's Seeds Alfalfa Sprouting Seeds, packaged in heat-seale
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
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Pacific Health Sciences Llc recalls Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptid
Undeclared shellfish (crab shell): source of ingredient Glucosamine sulfate
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TOJI CO. recalls Cloud Cafe branded Collagen Milk; Strawberry Milk Zero; Caff
Undeclared allergen ingredient (fish)
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TODD'S SEEDS LLC recalls Todd's Seeds Sprouting Seed Mix - Broccoli, Radish, Alfalfa,
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
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