Complete FDA and NHTSA recall records dated in 2020, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
The pump module keypad may exhibit keys that are unresponsive or stuck as a result of fluid ingress potentially resulting in a delay to the start of infusion, interruption of infusion, or…
Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer
One type of the ION Catheter Reprocessing Covers (PN 490114-02) has the potential to become disengaged or incorrectly engaged to the ION Fully Articulating Catheter which can result in…
There is an increased rate of potential false positive results for the Influenza A (no subtype) target, which may lead to 1) inappropriate antiviral use, 2) erroneous or delayed…
The Alaris PC unit can display incorrect syringe type and/or syringe sizes. This could result in delays in infusion, under-infusion, or over-infusion.
The linear shrinkage on the zirconia blank disc s part label is incorrect. The average linear shrinkage found on the product label was outside the acceptable range. The acceptable average…
The pump module keypad may exhibit keys that are unresponsive or stuck as a result of fluid ingress potentially resulting in a delay to the start of infusion, interruption of infusion, or…
Multiple or incorrect expiration dates were provided on the affected designation labels.
US-dates between the product package label and the bar code display.
Pump Module keypad may exhibit keys that are unresponsive or stuck as a result of fluid ingress potentially resulting in a delay to the start of infusion or interruption of infusion. Delays…
MicroPort Orthopedics Inc. is voluntarily recalling any existing inventory of PROFEMUR Titanium and Cobalt Chrome modular necks with previous package insert versions to replace the PROFEMUR…
undeclared soy (soy milk) allergen
Product may contain undeclared peanut butter.
Onions included various meal kits may be contaminated with Salmonella.
A foreign object found by a consumer in a chocolate bar.
Popcorn may contain foreign material: tempered glass between 3 mm and 7 mm in size
On August 28, 2020, the firm's customer discovered colored fibers up to 1/4 " in length after sifting a lot of finished carrageenan intended for use as an ingredient in a finished food…
The product contains undeclared milk.
Frozen cooked shrimp is possibly contaminated with Salmonella.
Product contains undeclared brazil nuts.
CGMP Deviations: Products manufactured at the same site were FDA testing found below the label claim for ethanol content and the presence of undeclared methanol.
Sub-Potent Drug: Out of specification test results for potency (below specification).
Labeling Not Elsewhere Classified: Product labeled to contain methanol
CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
