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All product recalls associated with CUSHMAN.
Total Recalls
1000
Past Year
896
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.
Textron Specialized Vehicles (Textron) is recalling certain 2024 Crushman Hauler Pro LSV vehicles equipped with the triple battery pack configuration. The dump bed latch may contact the top battery, cracking or puncturing the case.
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
Cummins, Inc. (Cummins) is recalling certain 2023-2024 Power Generation C275D2RE trailers. The vibration damper cap screws may be improperly tightened, which may cause the damper to separate from the engine.
Organic Yogi Echinacea Immune Support product is recalled because pesticide residues were detected above action levels.
CGMP Deviations
Labeling error. The 5-MTHF 1mg label incorrectly declares 5000mcg Folic Acid instead 1000mcg Folic Acid per serving in the Supplement Facts, but correctly declares Folate 1667mcg DFE. The front label correctly declares product as 5-MTHF Methyltetrahydrofolate 1mg (or 1000mcg).
Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot 540287. It was confirmed that Lot 540287 and Lot 508287 were swapped between the pouching and final pack.
A possible sterility issue (e.g. a breach in sterile packaging) was detected in Coloplast's facility on some ureteral dilator products. This issue on the ureteral dilator packaging has been identified during testing in our facility.
System error messages may delay the ability to test patient samples and the need for frequent calibration due to results outside the expected range when testing controls.
Forest River, Inc. (Forest River) is recalling certain 2023-2024 Coachmen Prism PRC24MB motorhomes. The Federal Information label may indicate the incorrect number of seat belts installed, resulting in an incorrect cargo carrying capacity.
Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.
Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.
This recall involves model ECO TERRA Eco Terra Mattresses manufactured from Aug 5, 2022 to Aug 18, 2022. The mattresses are 10 inches thick with a top panel that is ivory and quilted. The side panel is brown knit quilted with horizontal lines, and the top and bottom tape edges are ivory. The manufacture dates and model name "ECO TERRA" are located on the mattress label, sewn into the cover.
Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.
undeclared peanut and soy not listed in contains statement.
Randox Laboratories has identified that Inorganic Phosphate in Calibration Serum Level 3, CAL2351 & CAL10388, is running with a negative bias on RX Series instruments compared to other methods.
Beckman Coulter manufacturing discovered cracks around a threaded insert on the bottom of the Internal Wash Buffer Tank that is used within the Wash Buffer Supply Drawer on the DxI 9000.This can result in leaking, leading to delays in reporting patient test results, exposure to physical and chemical hazards, and damage to equipment or the environment.
Specific lots of Neria Soft Infusion Sets, which have been shipped into the US Market, have been shipped with the incorrect Instruction for Use (IFU) within the final pack. The IFU included is the IFU registered for the Rest of World (ROW) countries. The difference between the US IFU and the ROW IFU is the addition of an intended use section in the ROW IFU.
Customer complaints were received regarding falsely elevated results for some patient samples. Internal studies with customer return samples confirmed potential interactions that may lead to falsely elevated results when processed as below on the same instrument: " ARCHITECT Syphilis TP (LN 8D06) and/or ARCHITECT AdviseDx SARS-CoV-2-IgG II (LN 6S60) precedes ARCHITECT Anti-HCV testing (LN 1L79). " Alinity i Syphilis TP (LN 07P60) precedes Alinity i Anti-HCV testing (LN 08P05).
Foreign object; metal and plastic shavings.