FoodApr 10, 2024
Kick Ash Products Door County Love Dark Chocolate Cherry Granola, 1lb, laminated recall — FDA F-1116-2024
Undeclared allergen (almond) in Dark Chocolate Cherry Granola
Class IFDA: TerminatedKick Ash Products 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 136
Records are ordered by the best available source date.
FoodApr 10, 2024
Turkana Food Sekeroglu Lokum Love Turkish Delight Mixed With Pistachio And recall — FDA F-1118-2024
Product contains Acid Red 18
Class IIFDA: TerminatedTurkana Food Inc.
FoodApr 10, 2024
Waiakea Hawaiian Volcanic Water Naturally Alkaline recall — FDA F-1117-2024
Consumer complaints involving floating particles.
Class IIFDA: TerminatedWaiakea Bottling Inc.
FoodApr 10, 2024
THE COCA-COLA COMPANY Powerade Zero Fruit Punch - 20oz PET bottles 24 pack, 8 recall — FDA F-1112-2024
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Class IIFDA: TerminatedTHE COCA-COLA COMPANY
FoodApr 10, 2024
Samsung Bean Sprout Soy Bean Sprouts in a package labeled in part: Sam Sung Soy recall — FDA F-1114-2024
Listeria monocytogenes.
Class IFDA: TerminatedSamsung Bean Sprout
FoodApr 10, 2024
THE COCA-COLA COMPANY Powerade Mountain Berry Blast - 20oz PET bottles 24 pack, 8 recall — FDA F-1113-2024
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Class IIFDA: TerminatedTHE COCA-COLA COMPANY
DrugApr 10, 2024
X-Gen Pharmaceuticals Cyclophosphamide for Injection, USP, 500mg/vial, Lyophilized recall — FDA D-0433-2024
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted…
Class IIIFDA: TerminatedX-Gen Pharmaceuticals Inc.
DrugApr 10, 2024
SSM Health Care St. Louis DBA SSM St. Clare FentaNYL citrate, 10 mcg in 0.9% Sodium Chloride recall — FDA D-0436-2024
Lack of Assurance of Sterility: Firm did not perform process validation.
Class IIFDA: OngoingSSM Health Care St. Louis DBA SSM St. Clare Health…
DrugApr 10, 2024
Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 recall — FDA D-0430-2024
Failed Dissolution Specifications: Out of Specification (OOS) was reported in test of dissolution at the 12th month time point in long term stability study.
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugApr 10, 2024
X-Gen Pharmaceuticals Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose recall — FDA D-0434-2024
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted…
Class IIIFDA: TerminatedX-Gen Pharmaceuticals Inc.
DrugApr 10, 2024
SSM Health Care St. Louis DBA SSM St. Clare Phenylephrine HCl, 1000 mcg/10 mL, 10 mL Total recall — FDA D-0435-2024
Lack of Assurance of Sterility: Firm did not perform process validation.
Class IIFDA: OngoingSSM Health Care St. Louis DBA SSM St. Clare Health…
Medical DeviceApr 3, 2024
Hologic Aptima CMV Quant Assay, Reference numbers: AW-22600-001, AW-25509-001, and recall — FDA Z-1371-2024
Use of assay along with plasma specimen may result in error code which would invalidate sample.
Class IIFDA: OngoingHologic, Inc.
Medical DeviceApr 3, 2024
InfuTronix Nimbus II Infusion System recall — FDA Z-1286-2024
InfuTronix is removing the Nimbus Infusion Pump Systems from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product…
Class IFDA: OngoingInfuTronix LLC
Medical DeviceApr 3, 2024
Boston Scientific POLARSHEATH Steerable Sheath 12F, REF M004CRBS3050 recall — FDA Z-1302-2024
Boston Scientific has identified a tooling error in manufacturing which may have caused delamination of the inner lumen of the sheath shaft in a subset of POLARSHEATH devices. This could…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceApr 3, 2024
InfuTronix Nimbus Administration Set recall — FDA Z-1285-2024
InfuTronix is removing the Nimbus Infusion Pump Systems from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product…
Class IFDA: OngoingInfuTronix LLC
Medical DeviceApr 3, 2024
Bruder Healthcare Company Thermalon Heating Pad, Item Number 24002 recall — FDA Z-1364-2024
Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
Class IIFDA: OngoingBruder Healthcare Company, LLC
Medical DeviceApr 3, 2024
Bruder Healthcare Company MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R recall — FDA Z-1367-2024
Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
Class IIFDA: OngoingBruder Healthcare Company, LLC
Medical DeviceApr 3, 2024
Bruder Healthcare Company Thermalon Eye Compress, Item Number 2434 recall — FDA Z-1359-2024
Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
Class IIFDA: OngoingBruder Healthcare Company, LLC
Medical DeviceApr 3, 2024
Bruder Healthcare Company MediBeads Neck Wrap, Item Number 34320 recall — FDA Z-1366-2024
Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
Class IIFDA: OngoingBruder Healthcare Company, LLC
Medical DeviceApr 3, 2024
Puritan Medical Products Company HydroFlock Sterile Flocked Collection Device, Part Number recall — FDA Z-1391-2024
It was discovered through a customer complaint that mislabeled product was distributed. Puritan distributed product labelled as 25-3317-H lot S1014 which contained product code 25-3317-U in…
Class IIFDA: OngoingPuritan Medical Products Company, LLC
Medical DeviceApr 3, 2024
Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140, facilitates femoral recall — FDA Z-1390-2024
Boston Scientific is conducting a removal of specific batches of the iSLEEVETM 14F Expandable Introducer Set due to complaints associated with a hemostatic valve leak.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceApr 3, 2024
Ortho-Clinical Diagnostics VITROS Performance Verifier II recall — FDA Z-1373-2024
The issue was mismatched diluent lots assembled into VITRO Chemistry Products Performance Verifier I and II. This issue has the potential to cause erroneous Quality Control (QC) results…
Class IIFDA: OngoingOrtho-Clinical Diagnostics
Medical DeviceApr 3, 2024
Baxter Supple Peri-Guard Repair Patch (new product codes): a) SPG0404, b) SPG0406, c) recall — FDA Z-1380-2024
A new contraindication was added to the IFU which states that Peri-Guard Repair Patch should not be used in neurosurgery since the product endotoxin level may be higher than the allowable…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceApr 3, 2024
Randox Laboratories Cystatin C Calibrator - In vitro diagnostic (IVD) use in the calibration recall — FDA Z-1369-2024
Cystatin C Calibrator Series CVS 2699, is running with a negative bias compared to other methods
Class IIFDA: OngoingRandox Laboratories Ltd.
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.