FoodJun 28, 2023
Fire Distributors Plus EARTH KRATOM TRAINWRECK 150 CAPSULES recall — FDA F-1000-2023
Products contain kratom, an unapproved food additive.
Class IIFDA: TerminatedFire Distributors Plus LLC
Latest records
Latest recalls — page 553
The newest recall records with useful source details are listed here.
FoodJun 28, 2023
Nutricia TYR Anamix Early Years infant formula Net Wt recall — FDA F-0989-2023
Infant formula contains undeclared tyrosine
Class IIFDA: TerminatedNutricia North America
FoodJun 28, 2023
Aquamar Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM recall — FDA F-0991-2023
Product found to contain undeclared wheat and eggs
Class IFDA: TerminatedAquamar Inc.
FoodJun 28, 2023
Aquamar Kanimi Crab Flavored Seafood Fancy Shred Style 92410 recall — FDA F-0992-2023
Product found to contain undeclared wheat and eggs
Class IFDA: TerminatedAquamar Inc.
FoodJun 28, 2023
ASK Foods Wegmans Penne Rigate Mozzarella Salad Net Wt 30 OZ recall — FDA F-0998-2023
Undeclared milk allergen
Class IIFDA: TerminatedASK Foods Inc.
FoodJun 28, 2023
Aquamar Miyako Select Shredded Crab Meat Keep Refrigerated #1485 recall — FDA F-0990-2023
Product found to contain undeclared wheat and eggs
Class IFDA: TerminatedAquamar Inc.
DrugJun 28, 2023
ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg, Unit Dose Carton 40 Capsules recall — FDA D-0893-2023
Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5…
Class IFDA: TerminatedThe Harvard Drug Group LLC dba Major Pharmaceuticals…
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992209 recall — FDA Z-1911-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Valve Repair Kit, REF: 4992306 Version A, Sterile EO, Rx Only recall — FDA Z-1916-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
Vyaire Medical bellavista 1000 Ventilator, Catalogue Number 301.100.030 recall — FDA Z-1966-2023
Vyaire Medical identified two patient safety risks during the use of the bellavista 1000 and bellavista 1000e: 1. Under certain conditions of use, the touchscreen may become unresponsive…
Class IIFDA: CompletedVyaire Medical
Medical DeviceJun 21, 2023
Vyaire Medical bellavista 1000e Ventilator, Catalogue Number 301.100.130 recall — FDA Z-1967-2023
Vyaire Medical identified two patient safety risks during the use of the bellavista 1000 and bellavista 1000e: 1. Under certain conditions of use, the touchscreen may become unresponsive…
Class IIFDA: CompletedVyaire Medical
Medical DeviceJun 21, 2023
Howmedica Osteonics Exeter V40 Trial Head, 26mm, -3, Catalog Number 6364-8-026 recall — FDA Z-1921-2023
The Exeter V40 Trial Head, catalog number 6364-8-026 (size 26mm, -3) may appear green, when it is meant to be a blue color. Green signifies a size 26mm, +3 Trial Head.
Class IIFDA: OngoingHowmedica Osteonics Corp.
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Drainage Catheter Insertion Tray 15.5F, REF: ASP-11-5, STERILE recall — FDA Z-1918-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
New Standard Device 'n'-Hole Post which is a component of the Revolution External Fixation recall — FDA Z-1824-2023
The threads on posts stripping out when tensioned during application process.
Class IIFDA: OngoingNew Standard Device Inc.
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992206 recall — FDA Z-1908-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
Boston Scientific Neuromodulation Driver Instrument, part of the Superion Indirect recall — FDA Z-1972-2023
Pending update to indirect decompression system instructions for use informing users that excessive force during the implant procedure may cause driver instrument tip breaks, which may…
Class IIFDA: OngoingBoston Scientific Neuromodulation Corporation
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992207 recall — FDA Z-1909-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Pleural Drainage Catheter Insertion Tray 15.5F, REF 4992508 recall — FDA Z-1914-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Pleural Drainage Catheter Insertion Tray 15.5F, REF 4992507 recall — FDA Z-1913-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
NOXBOX recall — FDA Z-1667-2023
Device may experience malfunctions due to misalignment of the check valve in the manifold. If the device fails, there is a risk of nitric oxide leak, oxygen gas leak, or earlier cylinder…
Class IFDA: TerminatedNOXBOX LTD
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992208 recall — FDA Z-1910-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Drainage Catheter Insertion Tray 15.5F, REF: ASP-15-5, STERILE recall — FDA Z-1920-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceJun 21, 2023
Ossur H / F Icelock 125 Ratchet, REF: L-125000 recall — FDA Z-1906-2023
A mechanical lock used to connect and release a locking liner into a prosthetic socket have an attachment pin and lock that can wear down faster than expected, leading to the potential for…
Class IIFDA: OngoingOssur H / F
Medical DeviceJun 21, 2023
Merit Medical Systems Aspira Pleural Drainage Catheter Insertion Tray 15.5F, REF 4992506 recall — FDA Z-1912-2023
There is a potential that valve assemblies will not open. preventing fluid from draining.
Class IIFDA: OngoingMerit Medical Systems, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 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 categories