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All product recalls associated with Seatex LLC.
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
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.
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Forest River, Inc. (Forest River) is recalling certain 2015-2017 Sanibel SNF3550 and 2021-2023 Sanibel SNF3902WB fifth wheels. The hitch (pin box) may not be sufficient for the Gross Vehicle Weight Rating (GVWR) and may fail.
Due to a manufacturing issue, device under process validation phase were inadvertently mixed into the main manufacturing process.
Screw heads, of pedicle screw systems, have thin lead-in thread that pose a risk of intraoperative cross-threading within the locking cap/screw head interface.
Users were experiencing the following error message (M-0B-125) stated Check Neutral Electrode Contact .
This recall involves select Frigidaire brand rear-controlled ranges produced from October 2023 through November 2023 with electronic control panels and the following model and serial numbers within these ranges: Model Number Serial Number Range FCRE3052BW VF34618193 thru VF34618322 FCRE305CBW VF34601466 thru VF34601608 FCRG3051BB VF34508449 thru VF34508592, VF34521553 thru VF34521696, VF34521697 thru VF34521835 FCRG3051BW VF34504801 thru VF34504942 FCRE3062AB VF34424109 thru VF34424252 FCRG3052BW VF34510705 thru VF34510818 FCRE3052BB VF34414413 thru VF34414546, VF34600745 thru VF34600888, FCRE3052BS VF34413405 thru VF34413692 FCRE306CAS VF34410621 thru VF34410752 VF34410338 thru VF34410338, VF34413117 thru VF34413260, VF34512157 thru VF34512300, VF34512673 thru VF34512816, VF34519273 thru VF34519416 FCRG3051BS VF34316279 thru VF34316279. Consumers should visit https://www.frigidaire.com/en/frigidaire-recall-information to see if their specific serial number is included in this recall. The model and serial numbers are located in the drawer beneath the oven.
Due to incorrect calibrations and controls, their is a potential of incorrect reporting of lower %IS and molecular response values.
If the DIVA touch display generates touch inputs without user interaction, due to possibility of the erroneous acknowledgement of a patient alarm, there is a potential for a delay in the detection of a change in a patient condition which prompted the alarm to generate. Although unlikely, this could potentially result in a patient harm.
Cystatin C Calibrator Series CVS 2699, is running with a negative bias compared to other methods
Three lots of the Boot Assembly, Traction Device are being recalled due to due to a customer report of an incorrectly oriented locking pin which caused the boot to detach from the traction system. If an impacted device is used during surgery, the boot may detach from the traction system, potentially leading to patient harm and a delay in surgery.
L. mono contamination
CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex
DeRoyal manufactured and distributed Surgical Tracecarts that contain a Nurse Assist 16FR Silver Urine Meter Foley which were subsequently recalled.
Belmont Trailers LLC (Belmont) is recalling certain 2023-2024 FlatTrak trailers. The spindle mount may crack, resulting in the spindle mount and spindle arm separating.
Failed Impurities/Degradation Specifications: Out-of-specification test results.
Presence of foreign material in food (plastic)
Forest River, Inc. (Forest River) is recalling certain 2019-2024 Georgetown and FR3 Class A motorhomes. The liquid petroleum gas (LPG) tank mounting brackets may break, which can result in the LPG tank becoming dislodged and damaged.
Boston Scientific has identified a tooling error in manufacturing which may have caused delamination of the inner lumen of the sheath shaft in a subset of POLARSHEATH devices. This could result in the embolization of a fragment during use (such as flushing of the sheath or introduction of the dilator or ablation catheter).
Teleflex is initiating this voluntary recall for the above-mentioned products due to reports received indicating a potentially defective component. The complaints received relate to resistance of the guidewire handle/chamber during use. The possible immediate health consequences of the component issue are arterial vasospasm and vessel injury arising from multiple arterial punctures with repeated attempts.
CGMP Deviations: Out of specification for residual solvents.