FoodApr 23, 2025
DELICIAS DE LA ABUELA Arepas de Chocolo, Abuelas Food Company, Delicias de la recall — FDA F-0708-2025
Undeclared allergen: Soy lecithin, less than 2%
Class IIFDA: TerminatedDELICIAS DE LA ABUELA Inc.
Latest records
Latest recalls — page 238
The newest recall records with useful source details are listed here.
FoodApr 23, 2025
Grain Millers Rolled Oats packaged in Bulk Poly Supersacks packaged and recall — FDA F-0725-2025
Potential Foreign material (plastic)
Class IIFDA: TerminatedGrain Millers Inc.
FoodApr 23, 2025
Reser's Fine Foods Trader Joe's Hot Honey Mustard Dressing recall — FDA F-0704-2025
Undeclared peanuts, soy, sesame, and wheat.
Class IFDA: TerminatedReser's Fine Foods, Inc.
FoodApr 23, 2025
Rong Shing Trading NY LEMON PLUM recall — FDA F-0712-2025
Product contains cyclamates.
Class IIIFDA: TerminatedRong Shing Trading NY Inc.
DrugApr 23, 2025
Chattem Unisom, SleepMinis, Diphenhydramine HCl, Mini-Capsules, 25 mg, 60 Mini-Capsules recall — FDA D-0362-2025
CGMP Deviations; detection of Nitrosamine Drug Substance-Related Impurities (NDSRI), N-nitroso-desmethyl-diphenhydramine (n-dph), above the FDA Recommended Intake Limit
Class IIFDA: OngoingChattem Inc
DrugApr 23, 2025
Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg/100 mL (10 mg/mL), 1 x 100mL recall — FDA D-0365-2025
LABELING: LABEL MIX-UP: The infusion bag is incorrectly labeled as Levetiracetam in 0.82% Sodium Chloride Injection 500 mg/100 mL, while the aluminum overwrap packaging correctly identifies…
Class IFDA: OngoingDr. Reddy's Laboratories, Inc.
DrugApr 23, 2025
Testosterone Cypionate Injection, USP, CIII, 200mg per mL recall — FDA D-0363-2025
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Class IIFDA: OngoingEugia US LLC
DrugApr 23, 2025
Direct Rx CIPROFLOXACIN OPHTH SOLUTION, 0.3% 5mL bottle recall — FDA D-0364-2025
Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
Class IIFDA: OngoingDirect Rx
VehicleApr 23, 2025
F-150 labels recall — NHTSA campaign 25V271000
Ford Motor Company (Ford) is recalling certain 2025 F-150 vehicles. The air bag warning label may be missing from the dashboard. As such, these vehicles fail to comply with the requirements…
labelsFord Motor Company
VehicleApr 18, 2025
Bronco upper ball joint recall — NHTSA campaign 25V260000
Ford Motor Company (Ford) is recalling certain 2025 Bronco vehicles. The front upper control arm ball joint nut may be missing or tightened improperly, allowing the front upper control arm…
upper ball jointFord Motor Company
VehicleApr 17, 2025
Acura MDX exterior lighting recall — NHTSA campaign 25V259000
Honda (American Honda Motor Co.) is recalling certain 2014-2020 Acura MDX vehicles. Moisture may enter the tailgate lid light assembly and wiring harness, which can cause the interior and…
exterior lightingHonda (American Honda Motor Co.)
Medical DeviceApr 16, 2025
Tornier S.A.S stryker Blueprint Mixed Reality Glenoid Box Lid, Catalog Number MRUE205 recall — FDA Z-1539-2025
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Class IIFDA: OngoingTornier S.A.S.
Medical DeviceApr 16, 2025
Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY, REF ACC010371C recall — FDA Z-1505-2025
Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.
Class IFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceApr 16, 2025
Agilent Technologies GenetiSure Dx Labeling Kit, REF: K1201-64105, contains human reference recall — FDA Z-1544-2025
DNA Labeling Kit for use in sample labeling to be hybridized to oligonucleotide microarrays has a component, Human Reference DNA Female aliquot, affected by a mosaic aberration that may…
Class IIFDA: OngoingAgilent Technologies, Inc.
Medical DeviceApr 16, 2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as recall — FDA Z-1458-2025
Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
Class IFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceApr 16, 2025
MEDLINE INDUSTRIES, LP - Northfield Wayson Hydrocolloid Models: 1) recall — FDA Z-1530-2025
There is a potential for the sterility of the device to be compromised.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceApr 16, 2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as recall — FDA Z-1456-2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula
Class IFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceApr 16, 2025
Tornier S.A.S stryker HoloBlueprint Application, Catalog Number MRUE001 recall — FDA Z-1542-2025
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Class IIFDA: OngoingTornier S.A.S.
Medical DeviceApr 16, 2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as recall — FDA Z-1459-2025
Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
Class IFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceApr 16, 2025
Tornier S.A.S stryker Blueprint Mixed Reality Instrument Check Block, Catalog Number recall — FDA Z-1537-2025
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Class IIFDA: OngoingTornier S.A.S.
Medical DeviceApr 16, 2025
Tornier S.A.S stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless recall — FDA Z-1534-2025
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Class IIFDA: OngoingTornier S.A.S.
Medical DeviceApr 16, 2025
Qapel Medical Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration recall — FDA Z-1512-2025
Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.
Class IFDA: OngoingQapel Medical Inc.
Medical DeviceApr 16, 2025
CareFusion 303 BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID BD PYXIS recall — FDA Z-1550-2025
Due to a software issue, when attempting to restock the automated dispensing cabinet, user have received the banner message "Stocking window has passed, or item has been removed from…
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceApr 16, 2025
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137 in vitro recall — FDA Z-1529-2025
Ground screws on Dxl 9000 PCB boards may cause electric shorts, leading to smoke and potentially delaying patient results. Smoke also poses a hazard to equipment and users.
Class IIFDA: OngoingBeckman Coulter, Inc.
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Recent recall archives
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September 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories