FoodApr 24, 2024
HandNatural H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA recall — FDA F-1162-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
April 2024 recalls — page 5
These records include useful source details for the selected month.
FoodApr 24, 2024
Weis Markets, Inc., Ice Cream Division Bakery Item Peanut Butter Filled Iced Donuts 6 ct recall — FDA F-1152-2024
Foreign material (metal) in donuts
Class IIFDA: TerminatedWeis Markets, Inc., Ice Cream Division
FoodApr 24, 2024
HandNatural H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE recall — FDA F-1172-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
FoodApr 24, 2024
HandNatural H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE recall — FDA F-1168-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
FoodApr 24, 2024
HandNatural H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE recall — FDA F-1167-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
FoodApr 24, 2024
HandNatural H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA recall — FDA F-1165-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
FoodApr 24, 2024
HandNatural H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE recall — FDA F-1169-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
FoodApr 24, 2024
Canadian Art Prints Tranquility & Teachings William Monague plate set, brand recall — FDA F-1175-2024
Product has been recalled because it may exceed FDA guidance levels for leachable lead.
Class IIFDA: TerminatedCanadian Art Prints
FoodApr 24, 2024
AROMITALIA USA Net Weight 123.46 oz, plastic container recall — FDA F-1153-2024
Coconut is declared in the ingredient list, but not declared in the contains statement in coconut paste.
Class IIIFDA: TerminatedAROMITALIA USA Inc.
FoodApr 24, 2024
HandNatural H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE recall — FDA F-1171-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
FoodApr 24, 2024
HandNatural H&NATURAL TEJOCOTE ROOT 90 PIECES, 3 MONTH SUPPLY, PURE AND recall — FDA F-1161-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
FoodApr 24, 2024
Shearer's Foods Great Value Twist & Shout Strawberry Creme Sandwich Cookies recall — FDA F-1174-2024
May contain foreign material (plastic)
Class IIFDA: TerminatedShearer's Foods, LLC
FoodApr 24, 2024
Weis Markets, Inc., Ice Cream Division Bakery Item Angel Creme Filled Chocolate Iced Donuts recall — FDA F-1151-2024
Foreign material (metal) in donuts
Class IIFDA: TerminatedWeis Markets, Inc., Ice Cream Division
FoodApr 24, 2024
HandNatural H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA recall — FDA F-1170-2024
Product recalled due to the presence of yellow oleander and its components in the product.
Class IFDA: OngoingHandNatural
DrugApr 24, 2024
Vancomycin Hydrochloride for Oral Solution, USP, 250 mg per 5 mL, packaged as (a) 80 mL recall — FDA D-0442-2024
Superpotent Drug: Due to overfilling of drug powder
Class IFDA: TerminatedAmneal Pharmaceuticals of New York, LLC
VehicleApr 23, 2024
Sorento wiring recall — NHTSA campaign 24V287000
Kia America, Inc. (Kia) is recalling certain 2024 Sorento vehicles. The motor driven power steering (MDPS) wiring harness may be incorrectly assembled, which can result in a loss of power…
wiringKia America, Inc.
Medical DeviceApr 17, 2024
RAYSEARCH LABORATORIES AB RayStation Software Version Numbers version numbers 8B, 9A, 9B recall — FDA Z-1482-2024
A use error that has occurred with RayStation/RayPlan, where material override using Silicon, Si, was incorrectly selected for a silicone gel polymer implant.
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
Medical DeviceApr 17, 2024
MEDLINE INDUSTRIES, LP - Northfield Bed Assist Bars, labeled as follows: a) Medline recall — FDA Z-1488-2024
Medline is recalling certain lots of our Adult Portable Bed Rails that were manufactured after the mandatory compliance requirement (ASTM F3186-17, Standard Specification for Adult…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceApr 17, 2024
PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from recall — FDA Z-1507-2024
Patient tabletop moved out to the home position during scan initialization, may cause operator/bystander staying by the rear of the table to collide with the moved tabletop and be injured
Class IIFDA: OngoingPhilips North America
Medical DeviceApr 17, 2024
Synovo Production ACETABULAR BEARING (xx)MM I.D X (xx) O.D recall — FDA Z-1497-2024
Medical device components were marketed without FDA clearance
Class IIFDA: OngoingSynovo Production
Medical DeviceApr 17, 2024
Baxter Healthcare Hillrom Welch Allyn Spot Vision Screener VS100, marketed under the recall — FDA Z-1510-2024
Baxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical standards.
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceApr 17, 2024
Baxter Healthcare Power Cords, marketed under the following models: a) CORD,METAL EARTH PIN recall — FDA Z-1511-2024
Baxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical standards.
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceApr 17, 2024
MEDLINE INDUSTRIES, LP - Northfield Bed Assist Bars, labeled as follows: a) Medline, Model recall — FDA Z-1487-2024
Medline is recalling certain lots of our Adult Portable Bed Rails that were manufactured after the mandatory compliance requirement (ASTM F3186-17, Standard Specification for Adult…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceApr 17, 2024
Synovo Production ACETABULAR FIXATION CUP, (xx)MM, 5 HOLE, Ti-6AI-4V ELI TiN CERAMIC recall — FDA Z-1496-2024
Medical device components were marketed without FDA clearance and without FDA approval
Class IIFDA: OngoingSynovo Production
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.