Complete FDA and NHTSA recall records dated in June 2020.
These records include useful source details for the selected month.
Software error was identified in the Pencil Beam Scanning (PBS) and Line Scanning (LS) dose calculation algorithms that could result in a local underestimation of expected dose.
Small but detectable holes in the sterilization wrap used with the firm's 8 mm endoscope sterilization trays and handheld camera sterilization trays could lead to a potential breach of…
Incorrect IOL diopter
potential risk that Legionella may be present in the Unity machine room, specifically the heat exchanger condensation collection tray.
There is a potential for the surgical system to detach from the operational room table unexpectedly. This could result in the surgical system falling onto the patient resulting in blunt…
A manufacturing error resulted in out of specification R3 Acetabular Shells
There is potential for the plastic optical tip to become detached from the metal shaft.
The presence of N-acetyl-p-benzoquinone imine (NAPQI), a metabolite of acetaminophen, may cause interference in certain chemistry assays when testing patient samples.
The bracket torque was mislabeled on the packaging.
There is a risk for a false mutation positive result in rare cases resulting from a fluorescence artefact. In these rare cases, the controls pass correctly, while a fluorescence artefact in…
World Flavors, Inc. initiated a recall of 085-CH-550-35 Cheese Whiz-Small Bag-No Art. Colors Lots 9280009, 9280010, 9280011, 9280012 and 025-BBQ-468 Barbeque Sauce Base Lot 9283079, because…
Potential Listeria monocytogenes contamination of Butternut Squash
Wild Harvest Organic Basil has the potential to be contaminated with Cyclospora cayetanensis.
Product contained an ingredient (farro) that potentially contain small stones.
World Flavors, Inc. initiated a recall of 085-CH-550-35 Cheese Whiz-Small Bag-No Art. Colors Lots 9280009, 9280010, 9280011, 9280012 and 025-BBQ-468 Barbeque Sauce Base Lot 9283079, because…
Failed dissolution specification - dissolution results of 59% (spec. NLT 85%) at the 24 month time point (end of shelf life).
Presence of Particulate Matter: particulate matter identified after reconstitution.
Presence of Particulate Matter - found in reserve sample vials at the firm.
Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.
Subpotent drug - Product did not contain drug.
Failed Impurities/Degradation Specifications: potential migration of benzophenone at very low level into the product from container.
Presence of Particulate Matter - found in reserve sample vials at the firm.
BMW of North America, LLC (BMW) is recalling certain 2019 Z4 sDrive30i, 2019-2020 330i xDrive, M340i and M340i xDrive, 2020 X3M and X4M, and Toyota Supra vehicles. In certain driving…
Mazda North American Operations (Mazda) is recalling certain 2020 CX-30 vehicles equipped with all-wheel drive. The evaporative vent hose for the fuel tank may be disconnected, possibly…
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.
