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
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 130
Records are ordered by the best available source date.
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
Medical DeviceApr 17, 2024
Boston Scientific EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral nutrition recall — FDA Z-1515-2024
Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceApr 17, 2024
Boston Scientific EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral recall — FDA Z-1516-2024
Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceApr 17, 2024
Intuitive Surgical Patient Cart, Part: 380601, a component of the da Vinci SP Surgical recall — FDA Z-1518-2024
Surgical system may have inadequately welded top and/or bottom belts in the link 2 of the entry guide manipulator assembly/instrument arm joints, that may cause the following, 1) Top…
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceApr 17, 2024
Microbiologics KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b, a) REF 0209P and recall — FDA Z-1483-2024
The positive control material (Rhizopus stolonifer) within the KWIK-STIK assembly was contaminated with another fungal organism (Aspergillus brasiliensis). As a result, users may observe A.…
Class IIFDA: OngoingMicrobiologics Inc.
Medical DeviceApr 17, 2024
Boston Scientific EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for enteral recall — FDA Z-1513-2024
Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceApr 17, 2024
Boston Scientific EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for enteral recall — FDA Z-1514-2024
Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceApr 17, 2024
Human Care Hc Sweden Ab Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer recall — FDA Z-1486-2024
Patient lift hanger bar may come loose, which could potentially pose risks to patients.
Class IIFDA: OngoingHuman Care Hc Sweden Ab
Medical DeviceApr 17, 2024
Baxter Healthcare Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Device recall — FDA Z-1509-2024
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
Synovo Production Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V ELI, TiN CERAMIC W/ PLASMA recall — FDA Z-1498-2024
Medical device components were marketed without FDA clearance
Class IIFDA: OngoingSynovo Production
Medical DeviceApr 17, 2024
ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing recall — FDA Z-1495-2024
The product does not meet sterility assurance level.
Class IIFDA: OngoingConvaTec, Inc.
Medical DeviceApr 17, 2024
Qiagen Sciences EZ2 Connect MDx-IVD Designed to perform automated isolation and purification recall — FDA Z-1508-2024
Insufficient welding leads to the heater cable becoming brittle and present with an error: ERROR 3481 HEATER UNABLE TO REACH TEMPERATURE; the instrument may stop, and the sample being…
Class IIFDA: OngoingQiagen Sciences LLC
About the 2024 recall archive
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.