Complete FDA and NHTSA recall records dated in March 2021.
These records include useful source details for the selected month.
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2018-2019 Atlas vehicles equipped with Continental tires. On the affected vehicles, it is possible that one or more tires…
Nissan North America, Inc. (Nissan) is recalling certain 2020-2021 Nissan Altima vehicles. The tie rod ball joint fastener was not tightened properly, which could result in the tie rod ball…
Kia Motors America (Kia) is recalling certain 2017-2021 Sportage and Cadenza vehicles. The electrical circuit in the Hydraulic Electronic Control Unit (HECU) may short-circuit, which can…
Medline Industries, Inc. is removing specific lots of STAT-Site Controls (Low and High) S-O303000, from the market, due to the product being compromised during shipment.
Smiths Medical became aware that three lot numbers of a specific model of Bivona Cuffless FlexTend" Tracheostomy Tube (model 60PFS45, lots 3991171, 3991172, and 3988103) may have been…
Due to complaints received that the tip/nose cone may detach from the Transcarotid Stent System.
A deformity affecting a specific lot of VITROS Chemistry Products VersaTips. Deformed VersaTips results may be biased by up to +/-16% for both immunometric and competitive assays.
incorrect device is contained in the package. The packaging label indicates that the device is for left side use, the product inside the package is for right side use. Use of an opposite…
Sternum saw blades within procedure packs are not sterile. The surgical saw blade has a green non-sterile sticker.
Misleading error messages and a gap in the Operator Manual which affects ARTIS Icono biplane or ARTIS Icono floor systems with software version VE20B. Potential issues include System error…
Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc Drapes from a single lot. A source for potential manufacturing error was identified and investigation is underway to…
An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.
Sternum saw blades within procedure packs are not sterile. The surgical saw blade has a green non-sterile sticker.
On January 7, 2021, STERIS identified that the glued bond between the beam and the leg spar assembly may begin to separate over time. This could result in unexpected movement of the…
Sternum saw blades within procedure packs are not sterile. The surgical saw blade has a green non-sterile sticker.
An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.
The external drainage system failed to meet Pyrogen test requirements for devices contacting cerebrospinal fluid of 2.15 endotoxins.
Due to unqualified "design verification" batteries being shipped to customers.
Potential for Clostridium botulinum. Products were produced and sold without licensure and regulatory oversight.
Small round fragments of plastic, the size of a dime, were found in the plastic bag during packaging. They had been left in the bag by the package manufacturer.
Undeclared anchovies
The firm received a consumer complaints that the product was spoiled.
undeclared cashews and almonds.
QA Allergen check by manufacturer noticed that Soy lecithin was not declared on the label.
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.
