Recalls in September 2026
322 recalls.
- Gluten Free EAT G.A.N.G.S.T.E.R Pizza Crust and Flat Bread Mix recall (GF Blends Inc)
FoodClass IReported November 4, 2026 · Products are recalled due to potential undeclared wheat gluten - Gluten Free Truly AIP Rustic Bread Mix recall (GF Blends Inc)
FoodClass IReported November 4, 2026 · Products are recalled due to potential undeclared wheat gluten - Gluten Free Truly AIP All Purpose Baking Mix Flour 15.3 oz recall (GF Blends Inc)
FoodClass IReported November 4, 2026 · Products are recalled due to potential undeclared wheat gluten - Sunny Sky Non-Dairy French Vanilla Creamer recall (Sunny Sky Products, LLC)
FoodClass IIReported November 4, 2026 · Product sterility was potentially compromised. - Miyoko's Creamery European Style Salted Plant Milk Butter recall (Prosperity Organic Foods Inc)
FoodClass IIReported November 4, 2026 · Product recalled due to yeast, mold, and E. coli. - ZestiGreens Broccoli Seeds for Sprouting & Microgreens recall (FORTUNA MARKETING, INC)
FoodClass IReported November 4, 2026 · Broccoli seeds potentially contaminated with Salmonella - Blue Bottle Coffee 4oz Sweet Blossom Simple Syrup in a glass boston round bottle with... recall (Pink House Alchemy, LLC)
FoodClass IIReported November 4, 2026 · Potential contamination with mold (Aspergillus niger) - Lidocaine Ointment USP recall (Direct Rx)
DrugClass IIReported November 4, 2026 · Subpotent Drug - Wechem Hand Guard8/1000mL Bag recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - SunCoast Paper Inc. Surgent Antiseptic Hand Soap recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Spurrier recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Chemseptic recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Pro Chem Suds Hand Soap recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - PRO CHEM BAN AID recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - PRO CHEM Fresh Start recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - People's FM-24 FOAMING High Foaming Antiseptic Hand and Body Wash recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Handtastic Foamy Mango Antiseptic Foam Soap Hand & Body Wash recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Lynx recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Lynx recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Lynx recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Antiseptic Hand Soap recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Delta Foremost Sani-Foam Mango recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Freshhands Premium Foamy Antibacterial Hand Soap Antiseptic recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Certus Medical Satin Foam recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Aero Foamy Mango Aloe Vera Antiseptic Hand & Body Wash recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Aerocare Sani Mango Antiseptic Hand and Body Wash recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Palm Antiseptic Hand Soap Net Contents: 1 Gallon recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Carevo recall (ARJOHUNTLEIGH POLSKA Sp. z.o.o.)
Medical deviceClass IIReported November 4, 2026 · The side support of the shower trolley may open unintentionally when the handles are not fully locked and additional force is applied during patient handling.... - Precision Pointer Electromagnetic recall (Stryker Leibinger GmbH & Co. KG)
Medical deviceClass IIReported November 4, 2026 · Device may fracture during use at the laser welded joint on the pointer tube. If this happens, loose parts may fall out of the product while the device is... - Nalu TD2 Therapy Disc with firmware recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported November 4, 2026 · Therapy Disc (TD) that powers and sends stimulation signals to an Implantable Pulse Generator (IPG), part of a neurostimulation system, has a firmware issue... - PENTAX Medical Water bottle assembly. Model Number. OS-H5. recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - PENTAX Medical Ultrasound Endoscope. Model Number. EG-3270UK. recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - PENTAX Medical Ultrasound Endoscope. Model Numbers. EG-3870UTK recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - PENTAX Medical Ultrasound Endoscope. Model Numbers. EG38-J10UT recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - PENTAX Medical Ultrasound Endoscope. Model Number. EG36-J10UR. recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - CareLink SmartSync Device Manager App recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Software problem has the potential for an inaccurate displayed longevity estimate. - CareLink SmartSync recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Software problem has the potential for an inaccurate displayed longevity estimate. - CareLink SmartSync Programmer recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Software problem has the potential for an inaccurate displayed longevity estimate. - EMAG system Model/Catalog Number: 418591/418591U Product Description: Nucleic acid... recall (BioMerieux SA)
Medical deviceClass IIReported November 4, 2026 · Delayed or no result when analyzing clinical samples with EMAG system (ref: 418591/418591U) due to a randomly occurring software error, Error 10003 Heater... - Model Number: 712010. recall (Philips North America)
Medical deviceClass IIReported November 4, 2026 · Potential for the device to fail immediately after an exposure, causing the system to remain stationary. - Orthoscan VERSA Accessory Cart recall (ZIEHM-ORTHOSCAN INC)
Medical deviceClass IIReported November 4, 2026 · The accessory cart weldment does not conform to weld dimensional specifications which may result in separation of the monitor arm mounting structure from the... - OmniaSecure Model 3930M recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Affected leads require additional engineering evaluation due to complaints regarding difficulty in achieving fixation during implantation. Potential harm of... - ETHILON Nylon Suture recall (Ethicon, LLC)
Medical deviceClass IIReported November 4, 2026 · Nylon suture indicated for use in general soft tissue approximation and/or ligation may have needles with distorted curvature, that may break during use, or... - Impella Connect Optical AIC recall (Abiomed, Inc.)
Medical deviceClass IReported November 4, 2026 · Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that... - Impella Optical Controller recall (Abiomed, Inc.)
Medical deviceClass IReported November 4, 2026 · Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that... - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported November 4, 2026 · Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that... - Gardners Basics brand Waltham 29 Broccoli Sprouting Seeds packaged in a white and... recall (Gardeners Basics)
FoodClass IReported October 28, 2026 · Salmonella - Wild West Seeds Broccoli Seeds Green Sprouting Calabrese lot #4105. Net Wt. 50lb. Wild... recall (Wild West Seed Inc)
FoodClass IReported October 28, 2026 · Salmonella - Evexias Health Solutions Amino Ultra recall (EVEXIAS HEALTH SOLUTION)
FoodClass IIReported October 28, 2026 · The product is mislabeled and fails to declare fish oil. - Marca El Pato Salsa para Enchiladas recall (Walker Foods, Inc)
FoodClass IIReported October 28, 2026 · Undeclared salt, garlic, and onions - Trader Joe's Crispy Rice Milk Chocolate Bar recall (Trader Joe's Company)
FoodClass IIReported October 28, 2026 · Undeclared wheat. Product outer label incorrect; contains wrong allergen ingredients. - Sempio Yellow Peach recall (Sempio Food Services, Inc)
FoodClass IIReported October 28, 2026 · elevated level of lead in canned peaches - GEARHARTS FINE CHOCOLATES Net Wt. 4oz recall (Gearharts Fine Chocolates, Inc.)
FoodClass IIReported October 28, 2026 · Foreign Object - Broken glass was found in a piece of finished product. - ARU recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - ARU recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - BB recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - BB recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations - evo recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - evo recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations. - Brush Buddies recall (PRITAM INTERNATIONAL PRIVATE LIMITED)
DrugClass IIReported October 28, 2026 · CGMP Deviations - Levoxyl recall (Pfizer)
DrugClass IIReported October 28, 2026 · Subpotent Drug: confirmed out-of-specification (OOS) assay during stability testing. - Levoxyl recall (Pfizer)
DrugClass IIReported October 28, 2026 · Subpotent Drug: confirmed out-of-specification (OOS) assay during stability testing. - Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30. recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 28, 2026 · A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications. - Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH31. recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 28, 2026 · A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications. - MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as: C-SECTION TRAY-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as: recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as: 1) LAPAROTOMY GYN CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as: 1) FETAL SURGERY CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as: C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE medical convenience kits labeled as: FETOSCOPY CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE DRAPE C-SECTION FEN CLR SCREEN W recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE DRAPE C-SEC FEN CLEAR SCRN WIRE recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - MEDLINE DRAPE C-SECTION W/POUCH ST 7/CS recall (Medline Industries, LP)
Medical deviceClass IIReported October 28, 2026 · Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. - Xact mole marker for mammography Model/Catalog Number: M15RM recall (Solstice Corporation)
Medical deviceClass IIReported October 28, 2026 · The radiopaque material may detach from the marker. In some cases, artifact was noted and attributed to the detached material. - InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT... recall (Medtronic Neuromodulation)
Medical deviceClass IIReported October 28, 2026 · Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may... - InterStim SureScan MRI Leads 978A1 & 978B1: LEAD 978A128 ISTM MICRO 28CM SSMRI... recall (Medtronic Neuromodulation)
Medical deviceClass IIReported October 28, 2026 · Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may... - Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported October 28, 2026 · A software defect in which existing users who had previously configured and enabled the long-acting dose reminder feature in version 1.2.0 or earlier... - Generic Name: restor3d MTP Implant Generic Name: MTP Implant Model/Catalog Number:... recall (restor3d Inc.)
Medical deviceClass IIReported October 28, 2026 · Implants were found in the field with orange sterilzation indicators which means implants were not exposed to sterilization. - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the...