FoodSep 20, 2023
Fantasy Cookie Trader Joe's Almond Windmill Cookies Buttery, tender cookies recall — FDA F-1508-2023
Foreign object; rocks.
Class IIFDA: TerminatedFantasy Cookie Corporation
September 2023 recalls — page 7
These records include useful source details for the selected month.
FoodSep 20, 2023
David Oppenheimer & Company I Zespri Organic Green Kiwi, product of New Zealand, one pallet recall — FDA F-1495-2023
Listeria monocytogenes
Class IFDA: TerminatedDavid Oppenheimer & Company I LLC
FoodSep 20, 2023
Twin City Foods Mixed Vegetables BEST PRICE TOPVALU, net per bag 500g recall — FDA F-1506-2023
Listeria monocytogenes
Class IIFDA: OngoingTwin City Foods, Inc.
FoodSep 20, 2023
Twin City Foods Individually Quick Frozen recall — FDA F-1504-2023
Listeria monocytogenes
Class IIFDA: OngoingTwin City Foods, Inc.
FoodSep 20, 2023
Twin Cities Co-Op Partners La Reyna Salsa Roja, Gluten Free / Medium recall — FDA F-1499-2023
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Class IIIFDA: TerminatedTwin Cities Co-Op Partners Inc.
FoodSep 20, 2023
Pegasus Foods Cream Cheese Rangoon NET WT: 5.00 LB recall — FDA F-1501-2023
Plastic foreign object found in product.
Class IIFDA: TerminatedPegasus Foods, Inc.
VehicleSep 20, 2023
General Motors rear recall — NHTSA campaign 23V642000
General Motors, LLC (GM) is recalling certain 2023 Cadillac Escalade, Escalade ESV, Chevrolet Suburban, Chevrolet Tahoe, GMC Yukon, and Yukon XL vehicles. The rear suspension outer control…
rearGeneral Motors, LLC
DrugSep 20, 2023
Pantoprazole Sodium for Injection 40mg per vial, Single dose vials NDC 71839-122-01 Packaged recall — FDA D-1148-2023
Lack of Assurance of Sterility: Powder discoloration due to small crack in some vials.
Class IIFDA: TerminatedBE PHARMACEUTICALS AG
DrugSep 20, 2023
Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle) recall — FDA D-1149-2023
Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results
Class IIFDA: TerminatedVistaPharm LLC
DrugSep 20, 2023
Hua Da Trading, Inc. dba Wefun WEFUN Capsules 825 mg, 1x10 blister pack per carton recall — FDA D-1180-2023
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil, an ingredient found in a FDA approved product for the treatment of male sexual…
Class IFDA: TerminatedHua Da Trading, Inc. dba Wefun Inc.
VehicleSep 18, 2023
Chrysler manual transmission recall — NHTSA campaign 23V641000
Chrysler (FCA US), LLC is recalling certain 2022-2023 Jeep Wrangler and Gladiator vehicles equipped with a manual transmission. The rearview camera may fail to display the rearview image…
manual transmissionChrysler (FCA US, LLC)
VehicleSep 15, 2023
Sorento camera recall — NHTSA campaign 23V639000
Kia America, Inc. (Kia) is recalling certain 2019 Sorento vehicles. Due to a manufacturing error, water may leak into the rearview camera, which can cause the rearview camera image not to…
cameraKia America, Inc.
Medical DeviceSep 13, 2023
Aesculap Implant Systems For intraventricular indications mainly used for operations within recall — FDA Z-2518-2023
Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30 neuroendoscope, a portion of the visual field is obscured.
Class IIFDA: OngoingAesculap Implant Systems LLC
Medical DeviceSep 13, 2023
Cook Lead Clipper- An auxiliary tool indicated for use in patients requiring percutaneous recall — FDA Z-2513-2023
Sterility of device may be compromised due to breach of the chevron seal of the packaging
Class IIFDA: OngoingCook Vandergrift, Inc.
Medical DeviceSep 13, 2023
Aomori Olympus Co Reusable distal attachments Models: MH-462, MH-463, MH-464, MH-465 recall — FDA Z-2523-2023
The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which exceeds the permissible exposure level calculated according to ISO 10993-17: 2002
Class IIFDA: OngoingAomori Olympus Co., Ltd.
Medical DeviceSep 13, 2023
Philips Ultrasound 3D9-3v Transducer, accessory to Philips Ultrasound Systems: EPIQ Elite recall — FDA Z-2517-2023
Transducer, an ultrasound system accessory, consists of two parts that are bonded together that may come apart due to chassis bonding issue, which may pose risk to users and patients of…
Class IIFDA: CompletedPhilips Ultrasound, Inc.
Medical DeviceSep 13, 2023
PARAGON VISION SCIENCES Fargo Ortho-K Lens recall — FDA Z-2516-2023
Manufactured lenses are not covered by existing FDA approval
Class IIFDA: OngoingPARAGON VISION SCIENCES, Inc.
Medical DeviceSep 13, 2023
Diversatek Healthcare ZVU Functional GI Software, REF: ZVU-3 recall — FDA Z-2521-2023
GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact revision 3.2.0.
Class IIIFDA: OngoingDiversatek Healthcare
Medical DeviceSep 13, 2023
Zimmer M/L Taper Hip Prosthesis Extended Offset, Reduced Neck Length, Size 4 recall — FDA Z-2519-2023
The outer package labeling and product etch are for a Size 6, however, the implant is a Size 4, and vice versa.
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceSep 13, 2023
Aomori Olympus Co Olympus Distal Attachment recall — FDA Z-2522-2023
The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which exceeds the permissible exposure level calculated according to ISO 10993-17: 2002
Class IIFDA: OngoingAomori Olympus Co., Ltd.
Medical DeviceSep 13, 2023
PARAGON VISION SCIENCES ISee Ortho-K Lens recall — FDA Z-2515-2023
Manufactured lenses are not covered by existing FDA approval
Class IIFDA: OngoingPARAGON VISION SCIENCES, Inc.
FoodSep 13, 2023
Nestle-USA Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz recall — FDA F-1491-2023
Potential presence of wood fragments.
Class IIFDA: TerminatedNestle-USA, Inc. (Corporate Office)
FoodSep 13, 2023
PBM Nutritionals Parent's Choice brand Sensitivity Premium Infant Formula recall — FDA F-1493-2023
Inadvertent release of rejected product to market
Class IIIFDA: TerminatedPBM Nutritionals, LLC
FoodSep 13, 2023
Cooperstown Cheese Company 1 recall — FDA F-1490-2023
Cheese may be contaminated with Listeria monocytogenes.
Class IIFDA: TerminatedCooperstown Cheese Company, 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.