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All product recalls associated with Calbiotech Inc.
Total Recalls
1000
Past Year
442
Class I (Serious)
138
Most Recent
Dec 2025
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.
The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, Calbiotech is fully committed to compliance with all State and Federal regulations.
The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, Calbiotech is fully committed to compliance with all State and Federal regulations.
The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, Calbiotech is fully committed to compliance with all State and Federal regulations.
The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, Calbiotech is fully committed to compliance with all State and Federal regulations.
The recall was initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. The firm reported although there is no potential health hazard related to this recall, the recall was initiated because Calbiotech is fully committed to compliance with all State and Federal regulations.
The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, Calbiotech is fully committed to compliance with all State and Federal regulations.
The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, Calbiotech is fully committed to compliance with all State and Federal regulations.
The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, Calbiotech is fully committed to compliance with all State and Federal regulations.
The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, Calbiotech is fully committed to compliance with all State and Federal regulations.
The Sun Smarties™ board skirts are peach microfiber with an embroidered flower accent and back pocket. Item number 13926 HIBI is printed on the care label inside the back of the waistband. The skirts were sold in girls' sizes 12 months to 4T. The skirts have six grommets, four on the front of the waistband and two on the back pocket.
The recall includes the following wooden full-size cribs: "Enchantment" (model #210), "Hush a Bye" (model #215), "Once upon a time" (model #320) and "Rock a bye" (model #1900-350). Only date codes from 0306 through 0308 are included in this recall. "Mother Hubbard's Cupboards", the model number and date code are printed on a label located on the bottom inside of the right side.
Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but cann
Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but can
Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but cann
Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but can
The Reebok Studio Cycle is an upright exercise bike used primarily in fitness centers and other institutional settings. The recalled bicycle is black with silver cranks. The unit has an internal belt drive. The base of the bicycle is a single piece that is welded to the frame. The legs are two straight horizontal bars with rounded edges. There is a logo located on the side of the exercise cycle that shows a person riding a bicycle.
The recalled Walther air cylinders for air pistols are aluminum and involve model 2/WALTHER 85 cm3, with the imprinted test date between 6 00 and 6 01 2000/2001 located on the end of the cylinder.
Potential for module to fail to obtain a NIBP reading on hypertension patients.
Telemetry Modules are failing to alarm for low heart rate and asystole.
During battery insertion there is potential for patient waveforms to move to an open receiver module or to an occupied receiver causing the intermittent inappropriate monitoring of both patients for several minutes.