FoodOct 4, 2023
Vitality Works 100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in recall — FDA F-1597-2023
Foreign material: pieces of a pen (writing utensil).
Class IIFDA: TerminatedVitality Works, Inc.
Monthly breakdown
2023 recalls by month
Select a month to review the recall records reported during that period.
December 2023295 records · 4 categoriesNovember 2023387 records · 4 categoriesOctober 2023214 records · 4 categoriesSeptember 2023253 records · 4 categoriesAugust 2023478 records · 4 categoriesJuly 2023263 records · 4 categoriesJune 2023339 records · 4 categoriesMay 2023410 records · 4 categoriesApril 2023189 records · 4 categoriesMarch 2023788 records · 4 categoriesFebruary 2023253 records · 4 categoriesJanuary 2023205 records · 4 categories
2023 recalls — page 38
Records are ordered by the best available source date.
FoodOct 4, 2023
Vitality Works 100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in recall — FDA F-1570-2023
Foreign material: pieces of a pen (writing utensil).
Class IIFDA: TerminatedVitality Works, Inc.
FoodOct 4, 2023
Vitality Works 100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in recall — FDA F-1552-2023
Foreign material: pieces of a pen (writing utensil).
Class IIFDA: TerminatedVitality Works, Inc.
FoodOct 4, 2023
Vitality Works 100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in recall — FDA F-1563-2023
Foreign material: pieces of a pen (writing utensil).
Class IIFDA: TerminatedVitality Works, Inc.
DrugOct 4, 2023
Eligard (leuprolide acetate) for injectable suspension, 7.5 mg every month, Sterile recall — FDA D-1178-2023
Superpotent Drug - Higher than expected levels of leuprolide acetate in the constituted product.
Class IIIFDA: TerminatedTolmar, Inc.
DrugOct 4, 2023
Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) recall — FDA D-1179-2023
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
Class IIIFDA: TerminatedRB Health (US) LLC
DrugOct 4, 2023
NEURACEQ Florbetaben F-18 (Neuraceq) Injection Solution 1.4 to 135 mCi/mL, 50 mL in 1 recall — FDA D-1177-2023
Lack of Assurance of Sterility: out-of-specification test results observed for Filter Integrity Test (FIT).
Class IIFDA: TerminatedSofie Co dba Sofie
VehicleOct 4, 2023
Atlas curtain recall — NHTSA campaign 23V671000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Atlas vehicles. The driver's side impact air bag may be missing a weld at the side air bag housing.
curtainVolkswagen Group of America, Inc.
VehicleSep 28, 2023
Chrysler display function recall — NHTSA campaign 23V654000
Chrysler (FCA US, LLC) is recalling certain 2022-2023 Ram 1500, Ram 3500 Cab Chassis with GVWR less than 10,000 lbs., and 2022-2024 Ram 2500 vehicles. The radio software may prevent the…
display functionChrysler (FCA US, LLC)
Medical DeviceSep 27, 2023
Avanos Medical COOLIEF RF Generator is an 80-watt Radio-Frequency (RF) Generator with four recall — FDA Z-2622-2023
Avanos has received an increase in complaints from customers for COOLIEF RF Generators producing F100 and F101 faults.
Class IIFDA: CompletedAvanos Medical, Inc.
Medical DeviceSep 27, 2023
Randox Laboratories Liquid Assayed Chemistry Control Premium Plus Level 3, Catalog Number recall — FDA Z-2609-2023
there has been a transcription error in the Instructions for Use (IFU) for the Liquid Assayed Chemistry Control Premium Plus Level 3. For Caeruloplasmin, the one and two standard deviation…
Class IIFDA: OngoingRandox Laboratories Ltd.
Medical DeviceSep 27, 2023
Abbott Medical Gallant HF Cardiac Resynchronization Therapy Defibrillator: HF CRT-D REF recall — FDA Z-2615-2023
Due to Bluetooth malfunction on a subset of Implantable Cardioverter Defibrillator (ICD) and Cardia Resynchronization Therapy Defibrillator *CRT-D) devices that were manufactured prior to…
Class IIFDA: OngoingAbbott Medical
Medical DeviceSep 27, 2023
Encore Medical DJO Surgical: Altivate Reverse, Humeral Stem, Small Shell, Size 6 x 108mm recall — FDA Z-2607-2023
Orthopedic device components were not subjected to final sterilization before shipment, which if implanted may lead to varying degrees of infection, which may require treatment, prolonged…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceSep 27, 2023
ETHICON PDS II (polydioxanone) Suture, Product Numbers Z844G-50, D10065-05, D10085-05 recall — FDA Z-2617-2023
Internal testing on returned product from this lot confirmed that some PDS" II (polydioxanone) Sutures from this lot did not meet tensile strength requirement.
Class IIFDA: OngoingETHICON, LLC
Medical DeviceSep 27, 2023
TyTek Tension Pneumothorax Access Kit TPAK10: 10 gauge, 3.25 inch- Intended for introduction recall — FDA Z-2611-2023
Updated IFU to inlclude: (1) identify the risks associated with the hazard of needle decompression and (2) improve the artwork showing placement site location
Class IIFDA: TerminatedTytek Medical Inc.
Medical DeviceSep 27, 2023
TyTek PneumoDart- Intended for introduction into the body to facilitate removal of air from recall — FDA Z-2612-2023
Updated IFU to inlclude: (1) identify the risks associated with the hazard of needle decompression and (2) improve the artwork showing placement site location
Class IIFDA: TerminatedTytek Medical Inc.
Medical DeviceSep 27, 2023
Smith & Nephew smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT recall — FDA Z-2621-2023
The firm conducting a recall due to a complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 4N LT implant instead of a LEGION NARROW PSvOXIN SZ 5N LT as…
Class IIFDA: OngoingSmith & Nephew Inc.
Medical DeviceSep 27, 2023
GE Medical Systems Information Technologies Prucka 3 Amplifiers, Model P1801PA, and Field recall — FDA Z-2613-2023
A diode on the power supply of the Prucka 3 Amplifier used with CardioLab/ComboLab systems could reach elevated temperatures and fail, then power off and become inoperable.
Class IIFDA: OngoingGE Medical Systems Information Technologies Inc.
Medical DeviceSep 27, 2023
Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Breakaway Nozzle & Prox recall — FDA Z-2600-2023
Potential for the Break-Away Femoral Nozzle the applicator tip connecting the cement cartridge, to disassemble or break off during use, can lead to the potential for loss of function of the…
Class IIFDA: OngoingStryker Corporation
Medical DeviceSep 27, 2023
Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Breakaway Nozzle & Solid recall — FDA Z-2599-2023
Potential for the Break-Away Femoral Nozzle the applicator tip connecting the cement cartridge, to disassemble or break off during use, can lead to the potential for loss of function of the…
Class IIFDA: OngoingStryker Corporation
Medical DeviceSep 27, 2023
Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway Nozzle, Restrictors recall — FDA Z-2601-2023
Potential for the Break-Away Femoral Nozzle the applicator tip connecting the cement cartridge, to disassemble or break off during use, can lead to the potential for loss of function of the…
Class IIFDA: OngoingStryker Corporation
Medical DeviceSep 27, 2023
O&M HALYARD FLUIDSHIELD 3 N95 Particulate Filter Respirator and Surgical Mask with SO SOFT* recall — FDA Z-2626-2023
One respirator sample failed a filtration efficiency test. This respirator may not provide adequate protection to the user.
Class IIFDA: OngoingO&M HALYARD, Inc.
Medical DeviceSep 27, 2023
Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway Nozzle, Restrictors recall — FDA Z-2602-2023
Potential for the Break-Away Femoral Nozzle the applicator tip connecting the cement cartridge, to disassemble or break off during use, can lead to the potential for loss of function of the…
Class IIFDA: OngoingStryker Corporation
Medical DeviceSep 27, 2023
Ortho-Clinical Diagnostics VITROS XT Chemistry Products TBIL-ALKP Slides recall — FDA Z-2623-2023
Samples containing high levels of ALKP (or an interfering substance) could deplete the available substrate in the reagent layer of a VITROS ALKP Slide and not post the substrate deleption…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
About the 2023 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.