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.
Incorrect device in the package. A package that was labeled as the CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9 (Part No. 3L93709 / Lot No. 5291990), contained the CORAIL HIGH OFFSET…
Central venous catheters may not fit over guide wire potentially causing procedure delay.
The contract supplier notified DePuy Synthes on June 16, 2017 that the kit expiration dates do not align with the earliest expiration date of the component lots within the kit. Some kit…
Abutments are unable to accept the final abutment screw
The ELAN 4 Air System was released to the market place prior to an authorized FDA 510K clearance. This issue does not affected sales outside the United States (OUS).
The affected AGC 2000 LP Patella products were over-molded leaving the outside diameter nonconforming to the print dimension.
B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI convenience kits containing the 22GA 1-1/2in SafetyGlide Needle due tothe presence of loose polypropylene foreign matter…
B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI convenience kits containing the 22GA 1-1/2in SafetyGlide Needle due to the presence of loose polypropylene foreign matter…
ELAN 4 burr/blade accessories were marketed without 510(k) premarket notification clearance.
The secondary supplier provided material was within specification but did not meet our design needs compared to the primary manufacturer. The product is designed for patient transfer, not…
Central venous catheters may not fit over guide wire potentially causing procedure delay.
The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.
Contamination with Methylbacterium thiocyanatum
ELAN 4 burr/blade accessories were marketed without 510(k) premarket notification clearance.
Torn sheath liner material was detected at the proximal end of the device during internal product testing which may be the result of damage incurred during the manufacturing process.
Lemon Ginger Syrup is recalled because the internal fill temperature of this product is not recorded.
Hibiscus Lavender Syrup is recalled because the internal fill temperature noted on production records was below 165¿F.
Gas developing in sealed bottle.
Firm is recalling multiple products following a supplier's recall of yeast ingredient due to potential contamination with metal fragments.
Label does not list sub-ingredients for mayo and sour cream The product contains undeclared egg, milk.
The firm was notified by a customer that the popcorn in the product contains grain beetles.
The firm was notified by the Ohio Dept. of Agriculture that they failed to include "soy lecithin" on their label.
Firm is recalling multiple products following a supplier's recall of yeast ingredient due to potential contamination with metal fragments.
Firm is recalling multiple products following a supplier's recall of yeast ingredient due to potential contamination with metal fragments.
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.
