FoodJul 12, 2023
Avery Brewing Company Gose con Sandia, Sour Ale with watermelon, limes and sea salt recall — FDA F-1021-2023
Due to over pressurization, can may fail/explode.
Class IIFDA: TerminatedAvery Brewing Company
July 2023 recalls — page 10
These records include useful source details for the selected month.
FoodJul 12, 2023
Cargill, Inc Corporate Headquarters Cargill Trisodium Citrate Dihydrate packaged in 50 lb recall — FDA F-1222-2023
Potential for foreign material (metal).
Class IIFDA: TerminatedCargill, Inc Corporate Headquarters
FoodJul 12, 2023
Cargill, Inc Corporate Headquarters Cargill Tripotassium Citrate Monohydrate packaged in 50 recall — FDA F-1223-2023
Potential for foreign material (metal).
Class IIFDA: TerminatedCargill, Inc Corporate Headquarters
FoodJul 12, 2023
PepsiCo Beverages & Foods Pearl Milling Company Self-Rising Yellow Corn Meal Mix Net Wt recall — FDA F-1229-2023
May contain trace amounts of undeclared milk
Class IIFDA: TerminatedPepsiCo Beverages & Foods
FoodJul 12, 2023
Stellex/CF Houston Wegmans single serve snack tray recall — FDA F-1225-2023
Undeclared almonds and/or undeclared wheat
Class IIFDA: TerminatedStellex/CF Houston, LLC
DrugJul 12, 2023
Tizanidine Tablets, USP, 4 mg, 100 Tablets recall — FDA D-0892-2023
Failed Dissolution Specifications: this repackaged product was recalled by the manufacturer, Dr. Reddy's Laboratories, Inc., due to out of specification results for dissolution.
Class IIFDA: TerminatedAmerisource Health Services LLC
DrugJul 12, 2023
Tizanidine Hydrochloride Tablet 4mg recall — FDA D-0894-2023
Failed Stability Specifications
Class IIFDA: OngoingPreferred Pharmaceuticals, Inc.
DrugJul 12, 2023
Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle recall — FDA D-0895-2023
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
Class IIFDA: TerminatedStrides Pharma Inc.
VehicleJul 12, 2023
Toyota Motor Engineering & Manufacturing column recall — NHTSA campaign 23V480000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2023 Corolla, Corolla Cross, Corolla Cross Hybrid, Highlander, Highlander Hybrid, Tacoma, 2023 Lexus RX350, RX350…
columnToyota Motor Engineering & Manufacturing
VehicleJul 11, 2023
Toyota RAV4 valve recall — NHTSA campaign 23V485000
Gulf States Toyota, Inc. (GST) is recalling certain 2023 Toyota RAV4 vehicles equipped with 17" black alloy accessory wheels. During installation of the alloy wheels, the tire valve stem…
valveGulf States Toyota, Inc.
Medical DeviceJul 5, 2023
Phadia US EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002) recall — FDA Z-2040-2023
Higher reported results when running EliA GliadinDP IgG Well on the instruments Phadia 2500EE compared to running EliA GliadinDP IgG Well on Phadia 250 instrument
Class IIFDA: OngoingPhadia US Inc.
Medical DeviceJul 5, 2023
Exactech Shoulder GPS Impactor Handle, Catalog #531-07-05 recall — FDA Z-2050-2023
The ball and spring housed within the locking mechanism of the handle can dislodge during disassembly or during impaction.
Class IIFDA: OngoingExactech, Inc.
Medical DeviceJul 5, 2023
Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG recall — FDA Z-2041-2023
Higher reported results when running EliA GliadinDP IgG Well on the instruments Phadia 2500EE compared to running EliA GliadinDP IgG Well on Phadia 250 instrument
Class IIFDA: OngoingPhadia US Inc.
Medical DeviceJul 5, 2023
Covidien Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS recall — FDA Z-2008-2023
Single ILLUMISITE Platform Console was converted from a 220-240VAC model to a 120VAC configuration using a non-supplied power cord and non-supplied fuses in the field by Medtronic Field…
Class IIFDA: OngoingCovidien, LLC
Medical DeviceJul 5, 2023
Permobil PushTracker E3 component utilized with the SmartDrive MX2+ Power Assist Device recall — FDA Z-2005-2023
When multiple processes are running on the watch's Central Processing Unit (CPU), the application may fail unexpectedly. If this happens, the motor on the power assist device continues to…
Class IIFDA: OngoingPermobil
Medical DeviceJul 5, 2023
Luminex Verigene Enteric Pathogens Nucleic Acid Test (EP), REF 30-002-023 recall — FDA Z-2023-2023
It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit (Part No. 20-005-022) and the VERIGENE Enteric Pathogens Nucleic Acid Test Kit (Part No. 20-005-023) could…
Class IIFDA: OngoingLuminex Corporation
Medical DeviceJul 5, 2023
Waldemar Link GmbH & Co. KG LINK Endo-Model Modular Knee Prosthesis System Femoral Segment recall — FDA Z-2048-2023
The firm discovered through customer complaints that device segments may not meet specifications.
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceJul 5, 2023
SEDECAL SA wDR 2.2 Mobile Digital Diagnostic X-Ray System recall — FDA Z-2045-2023
There is a software login in issue that may prevent the user from logging in.
Class IIFDA: OngoingSEDECAL SA
Medical DeviceJul 5, 2023
Waldemar Link GmbH & Co. KG LINK Endo-Model Modular Knee Prosthesis System Femoral Segment recall — FDA Z-2046-2023
The firm discovered through customer complaints that device segments may not meet specifications.
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceJul 5, 2023
Beckman Coulter Access Hybritech p2PSA reagent, REF B03704 and REF A49752 recall — FDA Z-2043-2023
Reagent lot numbers include an insufficient concentration of blocking reagent.
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceJul 5, 2023
Waldemar Link GmbH & Co. KG LINK Endo-Model Modular Knee Prosthesis System Femoral Segment recall — FDA Z-2049-2023
The firm discovered through customer complaints that device segments may not meet specifications.
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceJul 5, 2023
Hologic Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy samples recall — FDA Z-2035-2023
The inner needle of the Sertera device is either detaching or discharging and may cause delay in surgery
Class IIFDA: OngoingHologic, Inc.
Medical DeviceJul 5, 2023
Philips DigitalDiagnost C90, Model No. 712034 and 712035 recall — FDA Z-2042-2023
There is a software login in issue that may prevent the user from logging in.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceJul 5, 2023
Implant Direct Sybron Manufacturing LEGACY SMARTBASE, NE 3.0D 1MML, REF: 8730-81NE recall — FDA Z-2037-2023
Non-engaging abutments were distributed without FDA clearance; the performance characteristics have not yet been adequately established.
Class IIFDA: OngoingImplant Direct Sybron Manufacturing LLC
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.