Complete FDA and NHTSA recall records dated in 2019, 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 protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor component
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
The exposed area of fluo exams possibly does not match the active area of the detector within specified limits.
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
Philips has discovered through customer complaints and internal testing an intermittent electronic product defect in accordance with 21 CFR 1003.2(b)(1). When performing Cine runs, the…
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
These Instructions for Use has missing instructions related to the checking and changing of the application site procedure.
Reports of higher than anticipated positivity rate for patients tested using IgM Kit. Some negative samples may be reported as positive for IgM antibodies to Rheumatoid Factor.
The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter…
Firm discovered that yogurt peach yogurt may have incidental allergen (coconut) contamination.
Firm received notification of a positive L. mono test result from a random sample taken from of one our customer's retail locations by the Massachusetts Department of Public Health.
Firm received notification of a positive L. mono test result from a random sample taken from of one our customer's retail locations by the Massachusetts Department of Public Health.
Firm received notification of a positive L. mono test result from a random sample taken from of one our customer's retail locations by the Massachusetts Department of Public Health.
Firm received notification of a positive L. mono test result from a random sample taken from of one our customer's retail locations by the Massachusetts Department of Public Health.
Firm received notification of a positive L. mono test result from a random sample taken from of one our customer's retail locations by the Massachusetts Department of Public Health.
Product may contain undeclared milk.
Firm received notification of a positive L. mono test result from a random sample taken from of one our customer's retail locations by the Massachusetts Department of Public Health.
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.
