Complete FDA and NHTSA recall records dated in March 2021.
These records include useful source details for the selected month.
There is a risk that the device can start a fire if flammable liquids contact and enter the device.
Non-sterile product was shipped to customers labelled as sterile.
System may sporadically freeze (lock-up) during operation or while being in an idle state, no longer possible to interact with the system
Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.
There can be a potential breach of the sterile packaging barrier due to the development of pinholes at the crease of the double-folded edge of the current package configuration.
The text on the patient pack is correct and the product itself remains unchanged. FlexMedics does not expect device failures; Instead, there is an opportunity for misuse of the device if…
Due to the release of nonconforming Intraocular Lenses (IOLs).
Firm discovered that labeling had been switched for two products on one day of production - undeclared almonds and cashews.
Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1
Firm discovered that labeling had been switched for two products on one day of production - undeclared almonds and cashews.
Products are potentially contaminated with Salmonella.
Possible contamination with Cyclospora in basil
Defective Delivery System: Out of specification for mechanical peel.
Defective Delivery System: Out of specification for mechanical peel.
Defective Delivery System: Out of specification for mechanical peel.
Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Defective Delivery System: Out of specification for mechanical peel.
Presence of foreign tablets/capsules: Famotidine 20mg and ibuprofen 400mg tablets were found in a lot of famotidine 40mg.
Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and FP, Dihydroxy epoxy and Dieto epoxy impurities
Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.
Volkswagen Group of America, Inc. (Audi) is recalling certain 2021 Audi RS6 Avant, RS7, 2020-2021 A6 Allroad, S6 Sedan, S7, 2019-2021 A6 Sedan, and A7 vehicles. The score line on the…
Ford Motor Company (Ford) is recalling certain 2020 Lincoln Aviator and Ford Explorer vehicles. The rear lower control arm (RLCA) bolts that attach the rear lower control arms to the wheel…
BMW of North America, LLC (BMW) is recalling certain 2021 X5 sDrive40i, X5 xDrive50i, X5 M50i, X5 xDrive45e, 2021 X7 xDrive40i, X7 M50i, and XB7 vehicles. The head restraints on the…
Ford Motor Company (Ford) is recalling certain 2018 F-150, 2018-2020 F-250, F-350, and 2019 Escape vehicles equipped with Continental tires. On the affected vehicles, it is possible that…
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.
