FoodSep 25, 2024
KODIAK PROTEIN-PACKED POWER WAFFLES BUTTERMILK & VANILLA NET recall — FDA F-1814-2024
Foreign object - Soft plastic film
Class IIFDA: OngoingKODIAK CAKES LLC
September 2024 recalls — page 3
These records include useful source details for the selected month.
FoodSep 25, 2024
Flagstone Foods Wegmans PECAN BLEND NET WT 16OZ recall — FDA F-1819-2024
Undeclared Almonds. The firm was notified by their customer that the product contains undeclared almonds.
Class IIFDA: TerminatedFlagstone Foods LLC
VehicleSep 19, 2024
General Motors critical fasteners recall — NHTSA campaign 24V703000
General Motors, LLC (GM) is recalling certain 2023-2024 Chevrolet Colorado and 2023 GMC Canyon vehicles. The left or right front seat may have a seat belt buckle attachment bolt that was…
critical fastenersGeneral Motors, LLC
Medical DeviceSep 18, 2024
Medline Convenience kits, labeled as: 1) DYNJ39451D , Pack Number HOOD PACK recall — FDA Z-2985-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Smith & Nephew ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation recall — FDA Z-3096-2024
Product packaging process may result in an improper or incomplete seal of the outer foil pouch surrounding the inner Tyvek pouch, compromising product sterility
Class IIFDA: OngoingSmith & Nephew Inc.
Medical DeviceSep 18, 2024
Medline Convenience kits, labeled as: aa1) BURN PACK-LF, Pack Number DYNJ0781678S recall — FDA Z-3061-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) GER ARTH BASIN PK RFID-LF , Pack Number DYNJ0100999K recall — FDA Z-3018-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) C-SECTION TRAY, Pack Number AM160B recall — FDA Z-3048-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) URETEROSCOPY CDS SC-LF, Pack Number CDS983922F recall — FDA Z-3005-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) KIT GENERAL CLOSURE , Pack Number DYKMBNDL200A recall — FDA Z-3028-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: PARACERVICAL PUDENDAL BLOCK TR, Pack Number DYNJRA1023 recall — FDA Z-3014-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) ARTHROGRAPHY DRAPE PACK , Pack Number 00-399027M recall — FDA Z-3054-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline convenience kits containing semi-rigid suction liners labeled as follows: a) MINOR recall — FDA Z-3113-2024
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) FETOSCOPY CDS-LF, Pack Number CDS840215O recall — FDA Z-3004-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline ReNewal Reprocessed Ethicon Harmonic ACE+7 Shears w/ Adv recall — FDA Z-3095-2024
Potential for an incomplete seal on the packaging tray.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) DIALYSIS CATH ACCESS KIT, Pack Number DYNDA2516B recall — FDA Z-3011-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) LAVH CDS, Pack Number CDS760049AB recall — FDA Z-3046-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) PRESSURE TUBING B.I., Pack Number 81239 recall — FDA Z-3020-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Medline Convenience kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Code 613034700 recall — FDA Z-3053-2024
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Siemens Healthcare Diagnostics Atellica IM CA 19-9 (250 Test)- In vitro diagnostic use in recall — FDA Z-3101-2024
Positive bias for some samples around the CA 19-9 upper limit of normal of 35 U/m as compared to the previous lot. The sample bias observed was greatest in the Asia Pacific sample…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceSep 18, 2024
Medical Action Industries, Inc. 306 Foam Protective Pouches, model numbers 6010 recall — FDA Z-3129-2024
The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches…
Class IIFDA: OngoingMedical Action Industries, Inc. 306
Medical DeviceSep 18, 2024
Zimmer GmbH Biolox Option Taper Sleeve, Type 1 Taper, Standard Neck - Indicated for use in recall — FDA Z-3132-2024
Mislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck sleeve, and vice versa. The neck…
Class IIFDA: OngoingZimmer GmbH
Medical DeviceSep 18, 2024
Medline convenience kits containing semi-rigid suction liners labeled as follows: DENTAL recall — FDA Z-3108-2024
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceSep 18, 2024
Vit-l-escence Singles A3 recall — FDA Z-3066-2024
Due to a manufacturing issue, red particulates present in the expressed composite.
Class IIFDA: OngoingUltradent Products, 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.