Recalls in November 2025
177 recalls.
- Brand Name: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Processor ... recall (Advanced Bionics, LLC)
Medical deviceClass IIReported March 11, 2026 · Behind-the-ear sound processer packaging label is different then included product. - Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Yoyo Gummy Grape Plus Flavor recall (SB FOOD LLC)
FoodClass IIReported March 4, 2026 · The products contain an unallowed color Carmoisine (E122) - Acid Red 14. - Yoyo Gummy Tropical Flavor recall (SB FOOD LLC)
FoodClass IIReported March 4, 2026 · The products contain an unallowed color Carmoisine (E122) - Acid Red 14. - Yoyo Gummy Assorted Flavor recall (SB FOOD LLC)
FoodClass IIReported March 4, 2026 · The products contain an unallowed color Carmoisine (E122) - Acid Red 14. - Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 recall (Lotus Mom Corporation dba Indian Kitchen Mart)
FoodClass IReported February 25, 2026 · Potential contamination with leachable lead. - Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN INDIA SIZE 5 Sticker label:... recall (Lotus Mom Corporation dba Indian Kitchen Mart)
FoodClass IIReported February 25, 2026 · Potential contamination with leachable lead. - Brass Tope. Sticker label: $29.99+TAX recall (Lotus Mom Corporation dba Indian Kitchen Mart)
FoodClass IIReported February 25, 2026 · Potential contamination with leachable lead. - IKM Aluminum Saucepan 9" with Wooden Handle. Sticker label: ALUMINIUM PAN 2 SIDE... recall (Lotus Mom Corporation dba Indian Kitchen Mart)
FoodClass IIReported February 25, 2026 · Potential contamination with leachable lead. - Da Vinci 5 ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported February 25, 2026 · An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or... - Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. recall (Imu-Tek Animal Health, Incorporated)
FoodClass IIReported February 11, 2026 · Undeclared milk allergen - CINNAMON POWDER recall (VENZU TRADERS LLC)
FoodClass IIReported February 11, 2026 · Potential contamination with heavy metal (lead). - Brand Name: Molift Product Name: Molift 4-point sling bars recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift 2-point sling bars recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Vivoo Sodium Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo Vaginal pH Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo Protein Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo pH Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Exploro Highly Sensitive Male Fertility / Sperm Concentration Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Male Fertility Sperm Test for Home Use recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - S. Typhi/Para Typhi A Antigen recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Menopause Test Cassette recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - LH One Step Ovulation Test Device recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - LotFancy Urinary Tract Infection Urine recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Preserved Mustard in Soybean Oil recall (NEW WAY IMPORT INC)
FoodClass IIIReported February 4, 2026 · Undeclared allergen ingredient (wheat). - SIGMA Spectrum Infusion Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported January 28, 2026 · Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears. Due to its low viscosity, the defective... - Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 17.0.0 recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 16.0.0... recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 15.2.0 recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 10.1.1... recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 14.0.0 recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number:... recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - RayStation/RayPlan. Model/Catalog Numbers: 12.0.0 recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - RayStation/RayPlan. Model/Catalog Numbers: 11.0.0 recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - RayStation/RayPlan. Model/Catalog Number: 10.1. Software Version: RayStation/RayPlan... recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported January 28, 2026 · Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some... - MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed recall (Medline Industries, LP)
Medical deviceClass IReported January 28, 2026 · Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating... - MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed recall (Medline Industries, LP)
Medical deviceClass IReported January 28, 2026 · Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating... - MEDLINE beds labeled as: Full Electric Low Basic Homecare Bed recall (Medline Industries, LP)
Medical deviceClass IReported January 28, 2026 · Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating... - MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed recall (Medline Industries, LP)
Medical deviceClass IReported January 28, 2026 · Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating... - MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed recall (Medline Industries, LP)
Medical deviceClass IReported January 28, 2026 · Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating... - MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed recall (Medline Industries, LP)
Medical deviceClass IReported January 28, 2026 · Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating... - DPA161 Shrimp Paste recall (GUSTO GROUP, INC.)
FoodClass IIReported January 21, 2026 · Product tested high for lead. - Shrimp Paste recall (GUSTO GROUP, INC.)
FoodClass IIReported January 21, 2026 · Product tested high for lead. - Clindamycin Phosphate USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported January 21, 2026 · Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay. - BD Ready-to-Use Hydrophilic Catheter 14 Fr recall (HANGZHOU BEVER MEDICAL DEVICES CO., LTD.)
Medical deviceClass IIReported January 21, 2026 · Labeling error, Incorrect expiration date - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
Medical deviceClass IIReported January 21, 2026 · Emphasizing instructions for LVP duration programming located in the IFU. - FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle... recall (Abbott Diabetes Care, Inc.)
Medical deviceClass IReported January 21, 2026 · Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results - FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle... recall (Abbott Diabetes Care, Inc.)
Medical deviceClass IReported January 21, 2026 · Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results - FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle... recall (Abbott Diabetes Care, Inc.)
Medical deviceClass IReported January 21, 2026 · Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results - FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre... recall (Abbott Diabetes Care, Inc.)
Medical deviceClass IReported January 21, 2026 · Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results - EverRoast Chicken Caesar Wrap 85004224455 Net Wt: 11.25 oz recall (GBC Food Services, LLC)
FoodClass IReported January 14, 2026 · Potential presence of Listeria monocytogenes. - EverRoast Chicken Caesar Salad 850042244142 Net Wt: 8.5 oz recall (GBC Food Services, LLC)
FoodClass IReported January 14, 2026 · Potential presence of Listeria monocytogenes. - Locatelli Grated Pecorino Romano 48/8oz Shipper recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Ambriola Piccante grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Boar's Head Pecorino Romano Grated recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Sam's Pecorino Romano grated recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Boar's Head Grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Pinna Grated Pecorino Romano 2/10 recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Locatelli Grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup & lid recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK recall (Medline Industries, LP)
Medical deviceClass IIReported January 14, 2026 · Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient... - The Pressio 2 ICP Monitoring System recall (Sophysa)
Medical deviceClass IIReported January 14, 2026 · Customer complaints of Pressio monitor rebooting. - Philips Tempus Pro Patient Monitor recall (Remote Diagnostic Technologies Ltd.)
Medical deviceClass IIReported January 14, 2026 · Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If... - Beckman Coulter UniCel Dxl 800 recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported January 14, 2026 · Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard... - Beckman Coulter UniCel Dxl 600 recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported January 14, 2026 · Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard... - The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported January 14, 2026 · Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as... - Sheathes3D Seamless Viral Barrier recall (Sheathing Technologies Inc)
Medical deviceClass IIReported January 7, 2026 · Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk. - Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog... recall (Ferndale Laboratories, Inc.)
Medical deviceClass IIReported January 7, 2026 · Butyrate tube cracks during actuation, rendering product unusable. - Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe recall (Vortex Surgical Inc.)
Medical deviceClass IIReported January 7, 2026 · Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly. - Sinus Cap Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Pain Away Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Organic Ginger Root Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Ear Drops Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Chaga Mushroom Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Boswellia Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Baby Soothe Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Baby Allergy Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Anti-virus Herbal Supplement recall (A New Life Herbs, LLC)
FoodClass IIReported December 31, 2025 · Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label - Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz. recall (Silvestri Sweets Inc dba Carousel Candies)
FoodClass IReported December 31, 2025 · Undeclared pecan - Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag. 5 oz. recall (Silvestri Sweets Inc dba Carousel Candies)
FoodClass IReported December 31, 2025 · Undeclared wheat - Locatelli Pecorino Romano Cheese Grated recall (Wegmans Food Markets, Inc.)
FoodClass IReported December 31, 2025 · Product may be contaminated with Listeria monocytogenes. - Product: Zimi Kunefe Ready to eat recall (Karabetian Import and Distribution, Inc.)
FoodClass IIReported December 31, 2025 · partially hydrogenated oils (PHOs) in foods exported to the US - Product: Zimi Puff Pastry French Style recall (Karabetian Import and Distribution, Inc.)
FoodClass IIReported December 31, 2025 · partially hydrogenated oils (PHOs) in foods exported to the US