FoodMay 18, 2022
Eastland Food Bwell Bird's Nest Beverage Honey Flavor NET 8.45 FL OZ recall — FDA F-1053-2022
Deficient packaging material potentially leading to premature spoilage.
Class IIFDA: TerminatedEastland Food Corporation
May 2022 recalls — page 5
These records include useful source details for the selected month.
FoodMay 18, 2022
Eastland Food Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ recall — FDA F-1051-2022
Deficient packaging material potentially leading to premature spoilage.
Class IIFDA: TerminatedEastland Food Corporation
FoodMay 18, 2022
New Seasons Market packaged in a round plastic tub with lid, sold by various recall — FDA F-1072-2022
Potential foreign materials contamination.
Class IIFDA: TerminatedNew Seasons Market LLC
FoodMay 18, 2022
Ramen Hero - Vegan Shoyu ramen recall — FDA F-1057-2022
Affected lots of Vegan Shoyu Ramen meal kits used egg noodles which contain egg. The allergen of egg is not listed on the product label.
Class IFDA: TerminatedRamen Hero
FoodMay 18, 2022
Eastland Food Bwell Bird's Nest Beverage Sugar-Free Xylitol NET 8.45 FL OZ recall — FDA F-1056-2022
Deficient packaging material potentially leading to premature spoilage.
Class IIFDA: TerminatedEastland Food Corporation
DrugMay 18, 2022
Fagron SyrSpend SF Suspending Base, Cherry Flavored recall — FDA D-0856-2022
Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.
Class IFDA: CompletedFagron, Inc.
DrugMay 18, 2022
Mylan Institutional Esomeprazole Magnesium Delayed-Release Capsules, USP 40 mg recall — FDA D-0861-2022
Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.
Class IIFDA: TerminatedMylan Institutional, Inc. (d.b.a. UDL Laboratories)
DrugMay 18, 2022
Amgen MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 recall — FDA D-0855-2022
Defective container: loose crimp defect, potential loss of container integrity.
Class IIFDA: TerminatedAmgen, Inc.
DrugMay 18, 2022
buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 150 mg recall — FDA D-0857-2022
Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister…
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugMay 18, 2022
buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 200 mg, 60-count bottle recall — FDA D-0858-2022
Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister…
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugMay 18, 2022
Viatris Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle recall — FDA D-0854-2022
Failed Dissolution Specifications: low out of specification results for dissolution.
Class IIFDA: TerminatedViatris Inc.
DrugMay 18, 2022
Mylan Institutional Esomeprazole Magnesium Delayed-Release Capsules, USP 20 mg recall — FDA D-0860-2022
Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.
Class IIFDA: TerminatedMylan Institutional, Inc. (d.b.a. UDL Laboratories)
DrugMay 18, 2022
Lula Holdings Kill 'Dat Sanitizing Products Hand Sanitizer, 1 gallon (128 fl. oz.) 80% recall — FDA D-0859-2022
CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.
Class IIFDA: TerminatedLula Holdings LLC
VehicleMay 18, 2022
Palisade instrument cluster/panel recall — NHTSA campaign 22V353000
Hyundai Motor America (Hyundai) is recalling certain 2022 Palisade vehicles. The instrument cluster assembly may have been manufactured with excessive adhesive, which can disable the…
instrument cluster/panelHyundai Motor America
VehicleMay 17, 2022
Telluride instrument cluster/panel recall — NHTSA campaign 22V344000
Kia Motors America (Kia) is recalling certain 2022 Telluride vehicles. Excess adhesive in a circuit board within the instrument cluster may cause the instrument cluster display screen to be…
instrument cluster/panelKia Motors America
VehicleMay 13, 2022
Ford traction battery recall — NHTSA campaign 22V331000
Ford Motor Company (Ford) is recalling certain 2020 Escape and 2021 Lincoln Corsair vehicles equipped with 2.5L hybrid powertrains. Insufficient welds inside the high voltage battery may…
traction batteryFord Motor Company
VehicleMay 13, 2022
Mustang camera recall — NHTSA campaign 22V334000
Ford Motor Company (Ford) is recalling certain 2022 Mustang vehicles equipped with an Image Processing Module A (IPMA) or forward-facing camera. The camera is misaligned to the vehicle,…
cameraFord Motor Company
VehicleMay 12, 2022
Jeep Wrangler exterior lighting recall — NHTSA campaign 22V326000
Chryler (FCA US, LLC) is recalling certain 2022 Jeep Wrangler vehicles. The side marker lights may not function due to an incompatible tail light assembly wiring harness. As such, these…
exterior lightingChrysler (FCA US, LLC)
Medical DeviceMay 11, 2022
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion systems with software release R1.x recall — FDA Z-0886-2022
In the Azurion system, the user can add a new study to a patient by selecting the option Add Study . The Add Study dialogue box is then displayed where the Patient Type is selected to…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceMay 11, 2022
Siemens Healthcare Diagnostics Atellica IM Enhanced Estradiol (eE2) 100T - In vitro recall — FDA Z-1020-2022
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceMay 11, 2022
Siemens Healthcare Diagnostics ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro recall — FDA Z-1023-2022
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceMay 11, 2022
SML Distribution Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) recall — FDA Z-0944-2022
The product was distributed without FDA authorization or clearance for marketing and distribution in the US.
Class IFDA: OngoingSML Distribution, LLC
Medical DeviceMay 11, 2022
Siemens Healthcare Diagnostics Atellica IM Enhanced Estradiol (eE2) 500T - In vitro recall — FDA Z-1021-2022
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceMay 11, 2022
restor3d Evans Wedge Disposable Trials, Large Footprint, 8mm Thickness recall — FDA Z-1028-2022
During re-work of disposable instruments to relabel for 4-year shelf-life of disposable instruments, parts got mixed into other lots.
Class IIFDA: Terminatedrestor3d Inc.
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.