FoodJan 17, 2024
Eban's Bakehouse Sweet Indulgences - Peanut Butter Chocolate recall — FDA F-0699-2024
Undeclared Allergens - Milk and Soy
Class IFDA: TerminatedEban's Bakehouse 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 180
Records are ordered by the best available source date.
FoodJan 17, 2024
Garden Spot Foods, LLC Shiloh Farms Organic Salt Free 7 Grain Bread UPC recall — FDA F-0707-2024
Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
Class IIIFDA: TerminatedGarden Spot Foods, LLC.
FoodJan 17, 2024
Eban's Bakehouse Sweet Indulgences - Turtle Brownie recall — FDA F-0700-2024
Undeclared Allergens - Milk and Soy
Class IFDA: TerminatedEban's Bakehouse LLC
FoodJan 17, 2024
SUPREX Plant Based Nutrition. Carb & Sugar Block. Product Size: 120 Vegetable Cellulose recall — FDA F-0710-2024
FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
Class IIIFDA: TerminatedVita 360, LLC
DrugJan 17, 2024
buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg, 30-count bottles recall — FDA D-0222-2024
Presence of Foreign Tablets/Capsules
Class IIFDA: OngoingRising Pharma Holding, Inc.
DrugJan 17, 2024
Vigabatrin for Oral Solution, USP 500 mg per packet, 50 packets per box recall — FDA D-0220-2024
Defective Container: powder may leak out of the pouch
Class IFDA: CompletedInvaGen Pharmaceuticals, Inc.
Medical DeviceJan 10, 2024
Philips Respironics Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B recall — FDA Z-0638-2024
The following was missing from the Contraindications Statement: The AVAPS-AE therapy mode is contraindicated for invasive use and patients less than 10 kg. The AVAPS feature is…
Class IIFDA: OngoingPhilips Respironics, Inc.
Medical DeviceJan 10, 2024
Randox Laboratories SEROLOGY ToRCH lgM 2022 POSITIVE CONTROLI Intended for use with in vitro recall — FDA Z-0624-2024
A decrease in the reactivity of HSV Type 1/2 lgM in the Serology ToRCH lgM Positive Control when tested on the DiaSorin Liaison XL.
Class IIIFDA: OngoingRandox Laboratories Ltd.
Medical DeviceJan 10, 2024
Merit Medical Systems Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY recall — FDA Z-0629-2024
The sterility of microcatheter and infusion system devices cannot be guaranteed.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJan 10, 2024
Zimmer Biomet Spine Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with recall — FDA Z-0639-2024
Spinal fixation system 7.5mmx 50mm screws are packaged with the correct labeling, but the screws themselves were laser marked with an incorrect size description of 7.5 x 40; use of…
Class IIFDA: OngoingZimmer Biomet Spine Inc.
Medical DeviceJan 10, 2024
Busse Hospital Disposables Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE recall — FDA Z-0592-2024
Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance…
Class IFDA: OngoingBusse Hospital Disposables, Inc.
Medical DeviceJan 10, 2024
Abiomed Impella Connect, software portal for online device management that allows clinicians recall — FDA Z-0636-2024
The following features have been disabled from the web-based portal because the FDA has not evaluated these features for safety and effectiveness: Notifications via email feature; AIC alarm…
Class IIFDA: OngoingAbiomed, Inc.
Medical DeviceJan 10, 2024
Busse Hospital Disposables Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE recall — FDA Z-0593-2024
Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance…
Class IFDA: OngoingBusse Hospital Disposables, Inc.
Medical DeviceJan 10, 2024
Beaver Visitec International Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part recall — FDA Z-0632-2024
One lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceJan 10, 2024
Natus Medical External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only recall — FDA Z-0634-2024
Sterility assurance cannot be guaranteed for external drainage systems due to incomplete bioburden testing.
Class IIFDA: OngoingNatus Medical Inc.
Medical DeviceJan 10, 2024
Keystone Industries KeySplint Hard Clear - Indicated for the fabrication of orthodontic and recall — FDA Z-0630-2024
Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged with the wrong Instructions for Use. Keysplint Hard Clear were placed inside a zip lock bag along with KeySplint…
Class IIFDA: OngoingKeystone Industries
Medical DeviceJan 10, 2024
Natus Medical EDS 3 CSF External Drainage System, REF: NT821731C, STERILEEO, Rx only recall — FDA Z-0635-2024
Sterility assurance cannot be guaranteed for external drainage systems due to incomplete bioburden testing.
Class IIFDA: OngoingNatus Medical Inc.
Medical DeviceJan 10, 2024
Merit Pursue Microcatheter, REF: 28HC17130SN, 28HC17150ST/A, 29HC2015045/A, 29HC20150SN/A recall — FDA Z-0628-2024
The sterility of microcatheter and infusion system devices cannot be guaranteed.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJan 10, 2024
Busse Hospital Disposables Catalog No. 9251R1, 9251R2, 9251R3 TRACHEOSTOMY CARE SET / recall — FDA Z-0594-2024
Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance…
Class IFDA: OngoingBusse Hospital Disposables, Inc.
Medical DeviceJan 10, 2024
Beaver Visitec International Xstar Kojo Safety Slit Knife, 2.5mm 45 Bevel Up, Part Number recall — FDA Z-0633-2024
One lot of Part Number 373025, Xstar Kojo Safety Slit Knife 2.5mm 45 bevel up, incorrectly contains a bevel down blade instead of a bevel up blade.
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceJan 10, 2024
Insulet Omnipod 5 App recall — FDA Z-0591-2024
The bolus calculator is not recording the decimal point if it is the first value entered when changing a bolus dose. This may lead to an over-delivery of insulin to the user if the user…
Class IFDA: OngoingInsulet Corporation
Medical DeviceJan 10, 2024
Merit Maestro Microcatheter, Reference Numbers: 28MC2111045/B, 28MC21110ST/B, 28MC2113045/B recall — FDA Z-0627-2024
The sterility of microcatheter and infusion system devices cannot be guaranteed.
Class IIFDA: OngoingMerit Medical Systems, Inc.
FoodJan 10, 2024
Foremost Foods International Pamana Premium Bangus Belly recall — FDA F-0693-2024
Potential C. botulinum growth and toxin formation. Frozen bangus (milkfish) in reduced oxygen packaging does not contain instructions to keep frozen and instructions for proper thawing…
Class IIFDA: TerminatedForemost Foods International, Inc.
FoodJan 10, 2024
Foremost Foods International Pamana Premium Marinated Baby Bangus recall — FDA F-0691-2024
Potential C. botulinum growth and toxin formation. Frozen bangus (milkfish) in reduced oxygen packaging does not contain instructions to keep frozen and instructions for proper thawing…
Class IIFDA: TerminatedForemost Foods International, Inc.
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.