Byron White Formulas Recalls A-P Herbal Supplement Over Undeclared Walnuts
The FDA classified the recall as Class II, citing a label that does not declare walnuts in English.
Recalls & Safety Alerts in California
Every recalls & safety alerts report published for California, newest first.
FDA: Byron White Formulas Recalls A-L Complex Herbal Supplement Over Undeclared Walnuts
The Class II recall covers 18,791 units of the liquid supplement, distributed domestically and to ten foreign countries, according to an FDA enforcement report.
FDA Class I Recall Issued for Glutinous Rice Balls with Undeclared Peanuts
Khong Guan (HQ) recalls black and white glutinous rice balls with black sesame filling due to undeclared peanuts, a serious allergen risk.
FDA Reports Ongoing Recall of Byron White Herbal Supplement Over Undeclared Walnuts
The recall remains ongoing; consumers who have the product should check the lot codes.
FDA Class I Recall Issued for Glutinous Rice Balls with Undeclared Peanuts
Khong Guan (HQ) recalls 87 cases of frozen dessert dumplings sold in seven states due to undeclared peanuts.
Golden State Medical Supply recalls carbamazepine tablets over black specks
FDA classifies the action as Class II, citing CGMP deviations involving tablets with black specks.
Canon Medical recalls Alphenix X-ray systems over loose ceiling arm screws
FDA classifies the action as Class II, saying the screws may become loose and the chance of serious harm is remote.
FDA Class I recall issued for Addall XR Shot dietary supplement
ZMB Enterprises recalls Addall XR Shot after FDA finds undeclared stimulant and other ingredients.
FDA Class II Recall Issued for MicroVention BOBBY Balloon Guide Catheters
The FDA has classified a recall of 5,500 BOBBY Balloon Guide Catheters as Class II due to an increased rate of balloon pinhole defects.
FDA Designates IsoTis OrthoBiologics Recall as Class II
On August 5, 2026, the FDA classified the ongoing recall of 98 bone graft extender products as a Class II action.
FDA Reports Details on Ongoing Recall of Mellish Island Dietary Supplements
An FDA enforcement report published August 5, 2026, outlines an ongoing Class II recall of dietary supplements distributed by Mellish Island Corp.
FDA Closes Recall Action for Stryker Dual Spike Tube Sets
The agency considers the recall carried out for 2,739 units following reports of handpiece leaks.
Stryker Recalls Surgical Tube Sets Worldwide Over Handpiece Leak Reports
An ongoing FDA Class II recall covers 46,212 Stryker AHTO surgical tube sets distributed globally.
FDA Records Class II Recall for Big Way Hot Pot Miso Paste Over Undeclared Milk
Big Way Ca Inc has recalled 65 cases of hot pot miso paste distributed to two affiliated restaurants.
FDA Closes Recall of Beckman Coulter MicroScan Software Update
The agency considers the recall carried out for MicroScan LabPro V5.03 Panel Update 11 DVD Kits.
Freudenberg Medical Recalls Blom-Singer Voice Prostheses Over Mislabeled Packaging
FDA enforcement reports detail an ongoing Class II recall of 12 voice prosthesis units due to swapped packaging labels.
FDA Reports Class II Recall of Blom-Singer Voice Prostheses Over Packaging Swap
Freudenberg Medical, LLC has initiated an ongoing recall of 40 voice prosthesis units due to incorrect box labeling.
FDA Reports Class II Recall of Four Refurbished SNOO Smart Sleepers
An ongoing FDA Class II recall covers four pre-loved SNOO Smart Sleeper bassinets that failed quality standards prior to distribution.
FDA Lists Class I Recall of Bulk Organic Moringa Powder Over Salmonella
An FDA enforcement record shows Green Jeeva LLC recalled 2,490 kg of bulk Organic Moringa Powder after the ingredient tested positive for salmonella; the recall is listed as ongoing.
Amy's Kitchen Recalls 15,350 Cases of Organic Lentil Soup Over Potential Spoilage
An FDA enforcement report classifies the ongoing Class II recall of the 14.5 oz "light in sodium" soup, distributed in 28 states and Canada.
FDA Records Class II Recall of OLA-OLA Pounded Groundnuts for Undeclared Peanuts
An FDA enforcement record numbered H-1175-2026 lists 120 cases of the 32-ounce product, distributed in Texas, as recalled by Fayus Inc.; the recall status is ongoing.
Precision Dose Recalls Lot of Glycopyrrolate Oral Solution Over Unidentified Impurity
An FDA enforcement report dated July 29, 2026 lists the nationwide recall as ongoing and not yet classified.
FDA Lists Ongoing Class II Recall of Man Fon Won Ton Wrappers Over Undeclared Yellow #5 and #6
The agency's enforcement record cites 300 lbs of 10 oz refrigerated won ton wrappers distributed to California restaurants and, via a wholesaler, to New Mexico grocery stores.
FDA Lists Class II Recall of Penumbra RED 68 Reperfusion Catheter Over Possible Fracture
An ongoing recall of the single-use hospital catheter, initiated 3 June 2026, covers five lots distributed across the United States and 14 other countries, according to the FDA enforcement record.
FDA Publishes Class II Recall for Alphatec SafeOp Patient Interface Over Software Fault
The enforcement record covers three units distributed in Texas, Missouri and Indiana and lists the action as ongoing.
FDA Lists Class II Recall of Man Fon Wonton Wrappers Over Unlabeled Wheat and Dyes; No Lot Codes Listed
An FDA enforcement report dated July 29, 2026 records an ongoing recall of unlabeled wonton wrappers distributed to California restaurants and, through a wholesaler, to New Mexico grocery stores. The record gives no lot numbers or date codes, and states the bags carry no ingredient labeling.
FDA Records Class II Recall of 13 Brain Flow-Diverter Implants Over Swapped Length Labeling
An FDA enforcement report lists Micro Therapeutics, Inc. recalling Pipeline Flex Embolization Devices whose labeled implant length does not match the implant inside; the action is listed as ongoing.
FDA Posts Class II Recall of Karl Storz Flexible Hysteroscope Kits Over Expired Single-Use Seal
An FDA enforcement report lists 45 kits recalled across 15 states because the packaged gynecology seal had passed its expiry date. The record carries no lot or serial numbers, so a matching catalogue number is the only identifier published; the action is listed as ongoing.
Medtronic Recalls MiniMed Go Diabetes App Over Alerts That Fail to Fire at Night
An FDA enforcement report classifies the ongoing Class II action, covering 3,465 units of the smartphone app, over missed-dose and high-glucose alerts that are not triggered at night under certain settings.
FDA Records Class II Recall of Six Brain Flow-Diverter Implants Over Mislabeled Lengths
An FDA enforcement report lists Micro Therapeutics, Inc. as recalling six units of the Pipeline Flex Embolization Device with Shield Technology after devices were labeled with the wrong implant length; the action is listed as ongoing.