Complete FDA and NHTSA recall records dated in 2018, 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 catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
"Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
The recalling firm determined that biased results may occur for specific VITROS Immunodiagnostic Products (MicroWell Assays) at biotin concentrations which are lower than indicated in the…
Potential for product sterility breach due to a compromised or pinched seal defect
The date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
Finished product labeling did not declare wheat.
Undeclared almonds on the labeling
Finished product labeling did not declare wheat.
Finished product labeling did not declare wheat.
Deep-pit Seasoning product is recalled due to undeclared wheat. In addition, the label declares lactose but did not declare milk.
Hash brown product, sold under brand Murry's is recalled because the product may contain small fragments of hard, clear plastic.
Undeclared milk and soy.
Finished product labeling did not declare wheat.
Finished product labeling did not declare wheat and color additives (Yellow #6, Red #3, and Red #40).
Finished product labeling did not declare wheat.
Product is misbranded. Bottles contain another product -GABA Calm Sublingual Orange tablets.
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.
