FoodJul 19, 2023
Garelick Farms Tampico brand Mango Punch recall — FDA F-1245-2023
Product contains undeclared Yellow 5.
Class IIFDA: TerminatedGarelick Farms LLC
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 75
Records are ordered by the best available source date.
FoodJul 19, 2023
Oregon Potato Company Rader Farms Organic Fresh Start Smoothie Blueberry recall — FDA F-1236-2023
Potential contamination with Hepatitis A.
Class IFDA: TerminatedOregon Potato Company
FoodJul 19, 2023
Wawona Frozen Foods 4 lb. plastic bags - 10 bags per case Keep Frozen Item# 684779 UPC: 0 recall — FDA F-1231-2023
Product may contain Hepatitis A
Class IFDA: TerminatedWawona Frozen Foods Inc.
DrugJul 19, 2023
Tenn South Distillery LLC dba Big Machine Big Machine Distillery Hand Sanitizer Non-Sterile recall — FDA D-0915-2023
CGMP Deviation: impurities exceed allowable limits.
Class IIFDA: OngoingTenn South Distillery LLC dba Big Machine Distillery
DrugJul 19, 2023
SUNMARK EYE DROPS ORIGINAL FORMULA Original Eye Drops recall — FDA D-0897-2023
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
Class IIFDA: OngoingK.C. Pharmaceuticals, Inc.
DrugJul 19, 2023
Global Pharma Healthcare Private Delsam Pharma's ARTIFICIAL TEARS recall — FDA D-0922-2023
CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be…
Class IIFDA: OngoingGlobal Pharma Healthcare Private Limited
DrugJul 19, 2023
Atropine Sulfate Injection, USP 8 mg per 20 mL (0.4 mg per mL), 20 mL Multiple Dose Vials recall — FDA D-0917-2023
Presence of Particulate Matter: Particulate matter identified as fiber.
Class IIFDA: TerminatedAccord Healthcare, Inc.
DrugJul 19, 2023
Global Pharma Healthcare Private Artificial Tears recall — FDA D-0920-2023
CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be…
Class IIFDA: OngoingGlobal Pharma Healthcare Private Limited
DrugJul 19, 2023
Albuterol Sulfate Inhalation Aerosol, 90 mcg, 200 Metered Inhalation, net content 6.7 g recall — FDA D-0938-2023
Defective container: empty inhaler and leakage observed through the inhaler valve due to partially missing bottom seat (gasket).
Class IFDA: TerminatedCipla USA, Inc.
DrugJul 19, 2023
Global Pharma Healthcare Private Delsam Pharma's ARTIFICIAL TEARS recall — FDA D-0921-2023
Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Class IFDA: OngoingGlobal Pharma Healthcare Private Limited
DrugJul 19, 2023
Bivalirudin for Injection 250 mg, 10 Single-Dose Vials recall — FDA D-0918-2023
Presence of Particulate Matter: Particulate matter identified as fiber.
Class IIFDA: TerminatedAccord Healthcare, Inc.
DrugJul 19, 2023
Amlodipine Besylate Tablets, USP 10 mg, 1000-count bottles recall — FDA D-0899-2023
Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJul 19, 2023
Global Pharma Healthcare Private Artificial Tears recall — FDA D-0919-2023
Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Class IFDA: OngoingGlobal Pharma Healthcare Private Limited
DrugJul 19, 2023
Tiagabine Hydrochloride Tablets, 2 mg, 30-count bottle recall — FDA D-0914-2023
Failed Impurities: Out of Specification (OOS) result observed during Related Substances testing
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJul 19, 2023
Sunitinib Malate Capsules, 12.5 mg, 28-count bottles recall — FDA D-0913-2023
Failed Moisture Limits: Water (moisture) content above the approved product specifications.
Class IIFDA: TerminatedTeva Pharmaceuticals USA Inc.
DrugJul 19, 2023
EQUATE EYE DROPS DRY EYE RELIEF Dry Eye Relief Lubricant Eye Drops recall — FDA D-0898-2023
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
Class IIFDA: OngoingK.C. Pharmaceuticals, Inc.
VehicleJul 14, 2023
Tesla front recall — NHTSA campaign 23V488000
Tesla, Inc. (Tesla) is recalling certain 2021-2023 Model S and Model X vehicles. The front-row seat belts may not be connected properly to the pretensioner anchors, which can cause the seat…
frontTesla, Inc.
VehicleJul 14, 2023
Tesla camera recall — NHTSA campaign 23V489000
Tesla, Inc. (Tesla) is recalling certain 2023 Model S, Model X, and Model Y vehicles. The forward-facing camera may be misaligned, causing some of the active safety features such as…
cameraTesla, Inc.
Medical DeviceJul 12, 2023
Waldemar Link GmbH & Co. KG LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8 recall — FDA Z-2066-2023
Fixation screw was inserted through the wrong side of the augment (distal to proximal, as opposed to proximal to distal, which is the correct orientation).
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceJul 12, 2023
T.A.G. MEDICAL PRODUCTS CORPORATION BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use recall — FDA Z-2063-2023
Drill guides might bend when axial forces are applied by surgeon during procedure and result in potential metal shavings due to friction with the drill bit.Risk to patients includes…
Class IIFDA: OngoingT.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
Medical DeviceJul 12, 2023
Full Vision TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928 recall — FDA Z-2054-2023
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Class IIFDA: OngoingFull Vision Inc.
Medical DeviceJul 12, 2023
TEI Biosciences SurgiMend PRS; Collagen Matrix for Soft Tissue Reconstruction; Rx Only recall — FDA Z-2070-2023
Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
Class IIFDA: OngoingTEI Biosciences, Inc.
Medical DeviceJul 12, 2023
Full Vision TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927 recall — FDA Z-2053-2023
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Class IIFDA: OngoingFull Vision Inc.
Medical DeviceJul 12, 2023
Full Vision TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE recall — FDA Z-2056-2023
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Class IIFDA: OngoingFull Vision 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.