FoodApr 26, 2023
Power Selles Imports dba Culinary Collective Matiz Piparra Peppers are packaged in a clear recall — FDA F-0741-2023
A shard of glass being found in one of the jars.
Class IIFDA: TerminatedPower Selles Imports dba Culinary Collective
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 112
Records are ordered by the best available source date.
DrugApr 26, 2023
Amerisource Health Services Verapamil Hydrochloride Extended-Release Tablets, USP, 180 mg recall — FDA D-0536-2023
Failed Dissolution Specifications: Out of specification dissolution results above specified values.
Class IIFDA: TerminatedAmerisource Health Services LLC
DrugApr 26, 2023
Pharma Nobis Fast Acting Earwax Removal System (carbamide peroxide), 6.5%, 0.5 FL OZ (15 mL) recall — FDA D-0537-2023
CGMP Deviations: active ingredient may be subpotent before the labeled expiry due to degradation.
Class IIFDA: OngoingPharma Nobis LLC
VehicleApr 26, 2023
Kia instrument cluster/panel recall — NHTSA campaign 23V298000
Kia America, Inc. (Kia) is recalling certain 2023 Sportage, Sportage Hybrid, Sportage Plug-in Hybrid, Niro Hybrid, Niro Plug-in Hybrid, Soul, and Telluride vehicles equipped with a digital…
instrument cluster/panelKia America, Inc.
VehicleApr 25, 2023
Impreza switch recall — NHTSA campaign 23V292000
Subaru of America, Inc. (Subaru) is recalling certain 2023 Impreza vehicles. The brake light switch may be improperly adjusted and illuminate the brake lights without application of the…
switchSubaru of America, Inc.
VehicleApr 20, 2023
Ford lugs/nuts/bolts/studs recall — NHTSA campaign 23V283000
Ford Motor Company (Ford) is recalling certain 2023 Bronco and Ranger vehicles. The lug nuts on the driver's side wheels may have been improperly tightened.
lugs/nuts/bolts/studsFord Motor Company
Medical DeviceApr 19, 2023
Coloplast Manufacturing US Titan NB Infra Zero Ang 16cm, Catalog Number EN88162400 recall — FDA Z-1365-2023
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate…
Class IIFDA: OngoingColoplast Manufacturing US, LLC
Medical DeviceApr 19, 2023
Solta Medical thermage THERMAGE CPT SYSTEM REF TG-2B *** Solta Medical, Inc. thermage RF recall — FDA Z-1354-2023
A service unit was potentially improperly tested and calibrated during manufacturing on a failed test station.
Class IIFDA: OngoingSolta Medical Inc.
Medical DeviceApr 19, 2023
Coloplast Manufacturing US Titan Touch Pump, Catalog Numbers 5177502400 recall — FDA Z-1359-2023
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate…
Class IIFDA: OngoingColoplast Manufacturing US, LLC
Medical DeviceApr 19, 2023
Encore Medical EMPOWR Porous Knee Patella Over Drill, REF: 802-05-104 recall — FDA Z-1384-2023
Patella drills are marked with incorrect diameter size of 5.6mm, when they should be 5.4mm. Porous patella overdrills are marked with incorrect diameter size of 5.4 mm, when they should be…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceApr 19, 2023
Angiodynamics NanoKnife 5-Probe Procedure Pack 15 cm - Activation recall — FDA Z-1381-2023
Not programmed in accordance with specification. The programming affects the RFID function and does not allow the NanoKnife probes to be recognized by the NanoKnife generator resulting in a…
Class IIFDA: OngoingAngiodynamics, Inc.
Medical DeviceApr 19, 2023
Coloplast Manufacturing US Titan 0-Deg Scrotal 18 Cm, Catalog Number ES89182400 recall — FDA Z-1373-2023
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate…
Class IIFDA: OngoingColoplast Manufacturing US, LLC
Medical DeviceApr 19, 2023
Coloplast Manufacturing US Titan Touch NB Infr Zero 18cm, Catalog Number EN28182400 recall — FDA Z-1362-2023
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate…
Class IIFDA: OngoingColoplast Manufacturing US, LLC
Medical DeviceApr 19, 2023
Covidien Mild Chromic Gut Absorbable Sutures, CH GUT 5-0 12 UD SS-14 SS-14 (G-1766-K) recall — FDA Z-1389-2023
Medtronic was made aware of a supplier calibration issue during the contract sterilization process that may lead to unsterile product. Use of affected product may lead to an unspecified…
Class IIFDA: OngoingCovidien, LP
Medical DeviceApr 19, 2023
Howmedica Osteonics stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 5 RM/LL), REF 170615 recall — FDA Z-1385-2023
Ccertain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking
Class IIFDA: OngoingHowmedica Osteonics Corp.
Medical DeviceApr 19, 2023
Coloplast Manufacturing US Titan 0-Deg Scrotal 22 Cm, Catalog Number ES89222400 recall — FDA Z-1375-2023
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate…
Class IIFDA: OngoingColoplast Manufacturing US, LLC
Medical DeviceApr 19, 2023
Bio-Rad Laboratories BioPlex 2200, Anti-CCP Reagent Pack, REF 665-3250, IVD recall — FDA Z-1377-2023
Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on BioPlex 2200 Anti-CCP Kit (Lot 301481) stating that results were discrepant while performing lot-to-lot validation…
Class IIFDA: OngoingBio-Rad Laboratories, Inc.
Medical DeviceApr 19, 2023
Edwards Lifesciences Edward Lifesciences, REF 777F8, Swan-Ganz CCOmbo V, CCO/SvO2/CEDV/VIP recall — FDA Z-1379-2023
There is a potential that the distal end of the catheter may be bent beyond its intended curvature and when connected to patient monitoring device, the monitor may display an error message.
Class IIFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceApr 19, 2023
Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a next generation recall — FDA Z-1351-2023
An observed trend of high conductivity dialysate alarms in a hemodialysis system as a result of introducing a software tool into the manufacturing process.
Class IIFDA: OngoingOutset Medical, Inc.
Medical DeviceApr 19, 2023
Coloplast Manufacturing US Titan Touch Infr Zero Ang 22cm, Catalog Number ES28222400 recall — FDA Z-1368-2023
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate…
Class IIFDA: OngoingColoplast Manufacturing US, LLC
Medical DeviceApr 19, 2023
Covidien Plain Gut Absorbable Sutures, PLAIN GUT 5/0 18 P-13 X12 (SG-5686), PLAIN GUT 4-0 18 recall — FDA Z-1390-2023
Medtronic was made aware of a supplier calibration issue during the contract sterilization process that may lead to unsterile product. Use of affected product may lead to an unspecified…
Class IIFDA: OngoingCovidien, LP
Medical DeviceApr 19, 2023
Coloplast Manufacturing US Titan 0-Deg Infrapubic 20 Cm, Catalog Number ES88202400 recall — FDA Z-1372-2023
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate…
Class IIFDA: OngoingColoplast Manufacturing US, LLC
Medical DeviceApr 19, 2023
Coloplast Manufacturing US Titan Touch NB Infr Zero 16cm, Catalog Number EN28162400 recall — FDA Z-1361-2023
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate…
Class IIFDA: OngoingColoplast Manufacturing US, LLC
Medical DeviceApr 19, 2023
Covidien Chromic Gut Absorbable Sutures, SURGIGUT* 0 CHR GS-25 90CM X36 (CG-904), SURGIGUT* recall — FDA Z-1388-2023
Medtronic was made aware of a supplier calibration issue during the contract sterilization process that may lead to unsterile product. Use of affected product may lead to an unspecified…
Class IIFDA: OngoingCovidien, LP
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.