Recalls distributed in Kentucky – page 10

• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… recall
  FDA December 31, 2025 · Zimmer, Inc. · Class II
• LifeShield Drug Library Management (DLM), LifeShield Infusion Safety… recall
  FDA December 31, 2025 · ICU Medical, Inc. · Class II
• da Vinci 5, Surgeon Console Column Motor Connector recall
  FDA December 31, 2025 · Intuitive Surgical, Inc. · Class II
• BD Pyxis MedStation ES recall
  FDA December 31, 2025 · CareFusion 303, Inc. · Class II
• Grandma Belle's Tomato Basil Soup, Net Wt recall
  FDA December 31, 2025 · Lil Turtles LLC · Class II
• Alinity ci-series System Control Module (SCM) recall
  FDA December 24, 2025 · Abbott Laboratories · Class II
• Xpert¿ BCR-ABL Ultra Model recall
  FDA December 24, 2025 · Cepheid · Class II
• Xpert¿ BCR-ABL Ultra Model recall
  FDA December 24, 2025 · Cepheid · Class II
• InPen App, Model/CFN Number: MMT-8061 (Android Users) recall
  FDA December 24, 2025 · Medtronic MiniMed, Inc. · Class II
• BIOSURE HA SCREW, 6MM x 20 MM. Threaded metallic bone fixation fastener recall
  FDA December 24, 2025 · Smith & Nephew, Inc. · Class II
• Myosa for Kids KS1 recall
  FDA December 24, 2025 · Myofunctional Research Company USA · Class II
• AART Calf Implant Product Name: Calf Implant Model recall
  FDA December 24, 2025 · Dsaart LLC · Class II
• AART Pectoral Implant Product Name: Pectoral Implant Model recall
  FDA December 24, 2025 · Dsaart LLC · Class II
• AART Malar Implant Product Name: Malar Implant Model recall
  FDA December 24, 2025 · Dsaart LLC · Class II
• AART Chin Implant Product Name: Chin Implant Model recall
  FDA December 24, 2025 · Dsaart LLC · Class II
• AART Gluteal Implant Product Name: Gluteal Implant Model recall
  FDA December 24, 2025 · Dsaart LLC · Class II
• AART Silicone Carving Implant Product Name: Silicone Carving Implant Model recall
  FDA December 24, 2025 · Dsaart LLC · Class II
• DEXLOCK Achilles Repair Implant Kits, MAKT4520 recall
  FDA December 17, 2025 · Medline Industries, LP · Class II
• AMSCO 7053HP Washer/Disinfector Model recall
  FDA December 17, 2025 · Steris Corporation · Class II
• AMSCO 7052HP Washer/Disinfector Model recall
  FDA December 17, 2025 · Steris Corporation · Class II
• BD InLay Optima Ureteral Stent Kit Size: 8 Fr recall
  FDA December 17, 2025 · C.R. Bard Inc · Class II
• BD InLay Optima Ureteral Stent Kit Size: 6 Fr recall
  FDA December 17, 2025 · C.R. Bard Inc · Class II
• BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr recall
  FDA December 17, 2025 · C.R. Bard Inc · Class II
• Bard InLay Optima Size: 6 Fr recall
  FDA December 17, 2025 · C.R. Bard Inc · Class II
• CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer… recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System… recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer… recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• Sticker label (for Loose Bulk - peppermint peaches): 4401 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Sticker label (for Loose Bulk - peppermint peaches): 4401 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Sticker label (for Loose Bulk - white peaches): 4401 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Sticker label (for Loose Bulk - yellow peaches): 4044 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Sticker label (for Loose Bulk - yellow peaches): 4044 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• UPC 8 98429 00266 4 Peppermint Peach PROUCE OF U.S.A. 4 COUNT MIN. WT… recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• UPC 8 10248 03186 1 Peppermint Peach PRODUCE OF U.S.A. NET WT. 2 LBS… recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• UPC 8 10248 03186 1 WHITE PEACHES CALIFORNIA FRUIT PRODUCE OF U.S.A… recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A… recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• UPC 8 10248 03087 1 Peppermint Peach WHITE PEACHES READY TO EAT FROM… recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• UPC 8 10248 03165 6 YELLOW Peaches PRODUCE OF U.S.A. NET WT. 4 LBS… recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes… recall
  FDA December 17, 2025 · JR Simplot Company · Class II
• Reagent Kits/ containing flow cells, components of NextSeq 550Dx… recall
  FDA December 10, 2025 · Illumina, Inc. · Class II
• Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841 recall
  FDA December 10, 2025 · Philips Ultrasound, Inc · Class II
• Hemochron Activated Clotting Time Low-Range Test Cuvette recall
  FDA December 10, 2025 · Accriva Diagnostics, Inc. · Class II
• InSure ONE Fecal Immunochemical Test recall
  FDA December 10, 2025 · Enterix, Inc. · Class II