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All product recalls associated with Alchemee, LLC.
Total Recalls
1000
Past Year
899
Class I (Serious)
125
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.
Chemical contamination: Presence of benzene
Chemical contamination: Presence of benzene
Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.
Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
Cummins Inc. (Cummins) is recalling the high voltage battery packs in certain PowerDrive 7000 electric drivetrains. Pieces of the internal fasteners in the battery may detach, causing the battery pack to short circuit and fail.
Nerve Monitoring System with certain software versions has potential for increased stimulus artifact, which may require troubleshooting, and may lead to procedure delay, extubation, and medical intervention.
Levels of iodine exceeding label claim
Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
This recall involves the replacement reagent #1 bottles sold with Taylor Phosphate Test Kits #K-1106 and also sold separately. The kits are used to test the level of phosphate in water for pools, spas and aquariums. The water testing kits are labeled with the brand name "Taylor," the kit name "Phosphate Test" and part number "K-1106." The bottle in the kit that contains sulfuric acid is labeled with the brand name "Taylor," product name "Phosphate Reagent #1," part number "R-0980" and "A Size: 22 mL (.75 oz)." The replacement reagent bottle that is sold separately has the same label. Phosphate Reagent #1 has a shelf-life of 24 months.
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
Insulin pens may have been incorrectly assembled therefore users could experience the following: either the insulin cartridge will not fit into the cartridge holder; or the cartridge holder may be difficult to remove from the insulin pen. If the issue is present, and if the user does not have backup insulin they may experience temporary hyperglycemia.
There is a software issue that can permanently disable communication with an implantable neurostimulator (INS) when a specific intraoperative programming sequence is used.
Failed Dissolution Specifications: Out of specification results obtained during routine stability testing for dissolution.
CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the daily acceptable intake limit defined by the Food and Drug Administration.
Undeclared allergen (milk)
Undeclared allergen (milk)
Undeclared allergen (milk)
Five complaints received where surgeon was unable to remove and/or connect the inserter with the stem during surgery due to excess material remaining within the taper. Issue may lead to clinically significant extension of surgery to find a replacement.
During some clinical cases, it has been observed that the SO2 value may periodically appear as dashes on the Touchscreen Display indicating unavailable data. In these cases, a yellow low-limit alarm will also be triggered to the user, due to the dashed-out value.