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.
A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has an incorrect pad placed in the location of the leukocytes pad. This will result in control CB failure for…
The real-time numeric value for ventricular end-diastolic pressure (EDP) displayed on the Live Display may be inaccurate. Because ventricular pressure monitoring is only performed in the…
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding…
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding…
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding…
Significant design changes made to the Custom Skull Implant (CSI) devices, such as removing pressure relief holes across the length of the device and adding suture holes along the ridge of…
Software anomaly resulting in the loss of patient settings and stored patient data.
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding…
There is an error in the caddy artwork that misidentifies a specific plate and screw.
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding…
The cheese has the potential to be contaminated with Listeria monocytogenes.
The product test positive for peanut allergen which is not declared on the product label.
Products have the potential to be contaminated Clostridium botulinum.
The product test positive for peanut allergen which is not declared on the product label.
The product test positive for peanut allergen which is not declared on the product label.
The firm was notified that they failed to include the allergens milk & wheat in their ingredient statement.
The firm was notified by a customer that the product contains almonds and pecans that are not listed in the ingredient statement.
The product test positive for peanut allergen which is not declared on the product label.
Products have the potential to be contaminated Clostridium botulinum.
The product test positive for peanut allergen which is not declared on the product label.
The product test positive for peanut allergen which is not declared on the product label.
The product test positive for peanuts and almond allergen which is not declared on the product label.
The firm was notified by the State of TN that the product contained undeclared almonds.
The product test positive for almond allergen which is not declared on the product label.
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.
