Complete FDA and NHTSA recall records dated in November 2020.
These records include useful source details for the selected month.
The Printed Circuit Board Assembly (PCBA) are not in compliance with the IEC standard (60601 1, third edition). The BMU 40 units affected by this recall were designed with a short creepage…
When a Clot Detection Error is generated during the sample aspiration from the Primary Sample Tube the aspirated volume is dispensed into the first empty Secondary Sample Tube. This…
There is a potential for fire in the inside computer cabinet.
A potential issue of an incorrect CT scan delay timer to be displayed on the gantry Digital Display Panel (DDP) during multi-phase contrast scanning. This could lead the operator to receive…
A potential issue of an incorrect CT scan delay timer to be displayed on the gantry Digital Display Panel (DDP) during multi-phase contrast scanning. This could lead the operator to receive…
A potential issue of an incorrect CT scan delay timer to be displayed on the gantry Digital Display Panel (DDP) during multi-phase contrast scanning. This could lead the operator to receive…
A potential issue of an incorrect CT scan delay timer to be displayed on the gantry Digital Display Panel (DDP) during multi-phase contrast scanning. This could lead the operator to receive…
When a Clot Detection Error is generated during the sample aspiration from the Primary Sample Tube the aspirated volume is dispensed into the first empty Secondary Sample Tube. This…
Streptococcus culture medium contains an incorrect expiration date. The culture medium outer box labeling contains an expiration date of 2021-11-10 instead of the correct expiration date of…
In-house lab observations and customer reports of overheating and/or thermal damage to the battery pack, create the risk of exposure to smoke or hazardous materials, which may result in…
The recalling firm has observed an increase in complaints of problems encountered during the initial activation of the device in which the patient and/or the physician is unable or has…
The use of deionized water rather than distilled water during the manufacturing process, may have resulted in accelerated decreased OD signals for the Positive Control value.
Cervical Implants contain a label that incorrectly identifies the grade of titanium used.
A high frequency output (2 MHz) has not been cleared for distribution in the U.S.
The device may detect an incorrect Heater Bag volume which may lead to a 'Supply Bag Line Blocked' alarm during treatment. This alarm may cause the Heater Bag to contain more fluid than…
When a Clot Detection Error is generated during the sample aspiration from the Primary Sample Tube the aspirated volume is dispensed into the first empty Secondary Sample Tube. This…
Direct customer tested product upon receipt and had a positive result for Salmonella.
Wolfgang Confectioners, 50 E. 4th Avenue, York, PA 17404, has initiated a recall of Hu Almond Hunks and Hu Cashew Hunks, in 4 oz., stand up pouch, 6 bags per case because of mislabeled…
potential risk of Salmonella
CCP deviation associated with wash process, portion of affected product left company control.
potential risk of Salmonella
potential risk of Salmonella
potential risk of Salmonella
Wolfgang Confectioners, 50 E. 4th Avenue, York, PA 17404, has initiated a recall of Hu Almond Hunks and Hu Cashew Hunks, in 4 oz., stand up pouch, 6 bags per case because of mislabeled…
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
