Safety Recalls

17,567 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 6,101–6,150 of 17,567

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Medical Device Recall · September 11, 2025

  Ferno-Washington Inc

  FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.

  The fastening post hardware could loosen allowing the fastening post to detach from the cot

  Class II

• Food Recall · September 11, 2025

  E&E Foods Inc

  Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8-10oz, , item #991900011, individually Vacuum Package (IVP) portions in a plain white cardboard box, net wt. 10 lbs. per box. Product

  Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper.

  Class III

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Vehicle Recall · September 11, 2025

  Corp. Micro Bird, Inc.

  2025 MICRO BIRD G5 SCHOOL BUS

  The door panel may remain in the open position or open unexpectedly, increasing the risk of passenger being injured falling out of the bus.

  Unclassified

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Food Recall · September 11, 2025

  Harris Teeter

  Harris Teeter ASIAGO TEXAS TOAST, NET WT 5.0OZ (0.3lb), INGREDIENTS BREAD***CONTAINS WHEAT, UPC 0 72036 95364 3, Harris Teeter Raleigh, NC

  Undeclared Milk. During production the firm discovered that the ingredients "cheese and butter" is not listed in the ingredient statement and therefore the allergen milk was not listed in the contain statement.

  Class I

• Medical Device Recall · September 11, 2025

  Boston Scientific Corporation

  TENACIO Pump with InhibiZone; UPN: 72404429;

  The potential for devices to experience inflation and/or deflation performance issues or difficulties.

  Class II

• Medical Device Recall · September 11, 2025

  Insulet Corporation

  The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneous

  The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneously selecting a single number on the keyboard. This causes the single digit number to duplicate. This could result in errors in manual entry of digits - examples: bolus entry, I:C ratio, bolus calculator, prior to starting the bolus insulin delivery. Therefore, this may result in over delivery of insulin which may cause hypoglycemia.

  Class II

• Vehicle Recall · September 11, 2025

  Ford Motor Company

  2024 FORD BRONCO

  A fuel leak in the presence of an ignition source increases the risk of a fire.

  Unclassified

• Medical Device Recall · September 11, 2025

  Theken Companies LLC

  iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size

  Downstream recall for RES 97605, BioPro femoral components. Product failed transit testing. Impacted product may have potential issues with sterile barrier.

  Class II

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Consumer Product Recall · September 11, 2025

  Yiwu Shiyi Trading Co., Ltd., of China

  Children's Wooden Cactus Toys

  The recalled toy is intended for children under three years of age and contains small parts, which violates the small parts ban, posing a deadly choking hazard.

  Unclassified

• Consumer Product Recall · September 11, 2025

  VitaQuest International, LLC of Caldwell, New Jersey

  Bariatric Fusion Iron Multivitamin Bottles

  The recalled multivitamins contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The recalled packaging of the iron-containing multivitamins violates the federal standard for child-resistant packaging because the bottle caps are not child-resistant, posing a risk of deadly poisoning, if the contents are swallowed by young children.

  Unclassified

• Medical Device Recall · September 11, 2025

  Boston Scientific Corporation

  CX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404486 (15CM IP), (2) 72404488 (21CM IP);

  The potential for devices to experience inflation and/or deflation performance issues or difficulties.

  Class II

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC

  Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

  Class I

• Food Recall · September 10, 2025

  Gina Marie Bakery LLC

  Vanilla Cookies with Raspberry Peach Jam

  Undeclared Red 3 and Blue 1

  Class II

• Food Recall · September 10, 2025

  Gina Marie Bakery LLC

  Toasted Cherry Biscotti

  Contains undeclared Red 40

  Class III

• Medical Device Recall · September 10, 2025

  Medline Industries, LP

  Medline Adult Anesthesia Set, REF DYNJ39985G

  Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.

  Class II

• Medical Device Recall · September 10, 2025

  Abbott

  TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, FJ, (BiD Curve F-J), REF A-TFSE-FJ; cardiac catheter

  Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.

  Class I

• Food Recall · September 10, 2025

  Gooder Foods, Inc.

  GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS NET WT 6 OZ (170g) INGREDIENTS: GOODLES SHELLS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI,

  Undeclared allergens (cashews).

  Class I

• Food Recall · September 10, 2025

  Gina Marie Bakery LLC

  Vanilla Chocolate Dipped Cookies

  Undeclared Red 40

  Class III

• Food Recall · September 10, 2025

  GOOT ESSA, LLC

  Goot Essa, Der Mutterschaf Cheese, Sheep Tomme Style. 4 and 8 OZ. ( Pasteurized Sheep Milk, Salt, Vegetable Enzymes, Cheese Cultures ).

  The firm had a positive Listeria Monocytogenes on a sample from this batch of product made.

  Class I

• Food Recall · September 10, 2025

  Gina Marie Bakery LLC

  Toasted Almond & Cherry Biscotti

  Undeclared Red 40

  Class III

• Medical Device Recall · September 10, 2025

  Abbott

  TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DF, (BiD Curve D-F), REF A-TFSE-DF; cardiac catheter

  Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.

  Class I

• Food Recall · September 10, 2025

  Gina Marie Bakery LLC

  Italian Mixed Vanilla Cookies

  Undeclared Almonds, Sesame, Red 40, Red 3, and Blue 1

  Class II

• Vehicle Recall · September 10, 2025

  Harley-Davidson Motor Company

  2023 HARLEY-DAVIDSON RH1250S, 2024 HARLEY-DAVIDSON RH1250S

  An upper triple clamp that fractures while the motorcycle is being operated could lead to a loss of control, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · September 10, 2025

  Abbott

  TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, D, (UniD Curve D), REF A-TFSE-D; cardiac catheter

  Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.

  Class I

• Food Recall · September 10, 2025

  Gooder Foods, Inc.

  GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET WT 5.25 OZ (149g) INGREDIENTS: GOODLES SPIRALS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI,

  Undeclared allergens (milk).

  Class I

• Medical Device Recall · September 10, 2025

  Abbott

  TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, F, (UniD Curve F), REF A-TFSE-F; cardiac catheter

  Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.

  Class I

• Food Recall · September 10, 2025

  Gina Marie Bakery LLC

  Italian Sesame Cookies

  Undeclared Sesame, Undeclared Yellow 5, Red 40, Yellow 6

  Class II

• Medical Device Recall · September 10, 2025

  Abbott

  TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DD, (BiD Curve D-D), REF A-TFSE-DD; cardiac catheter

  Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.

  Class I

• Food Recall · September 10, 2025

  Gina Marie Bakery LLC

  Vanilla with Apricot Jam Cookies

  Undeclared Red 40 and Yellow 6

  Class II

• Food Recall · September 9, 2025

  Hale inc

  Lotsa Pasta International Food Shop Fresh Basil Infused Olive Oil, Net Wt. 12 oz. (375ml), packaged in a glass bottle, UPC 736211448316, packed 12 bottles per case

  Potential to be contaminated with Clostridium botulinum. Products manufactured without an approved process filed.

  Class II

• Food Recall · September 9, 2025

  WFM Purchasing, LP

  Whole Foods Market Blueberry Almond Granola, PLU 86032, packaged in a clear plastic container.

  Product was incorrectly labeled, resulting in undeclared wheat, sesame, and cashew.

  Class I

• Medical Device Recall · September 9, 2025

  NOXBOX LTD

  NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I

  The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for the device to respond to user prompts.

  Class I

• Food Recall · September 9, 2025

  Hale inc

  Lotsa Pasta International Food Shop Roasted Garlic Infused Olive Oil, Net Wt. 12 oz. (375ml), packaged in a glass bottle, UPC 736211448415, packed 12 bottles per case

  Potential to be contaminated with Clostridium botulinum. Products manufactured without an approved process filed.

  Class II

• Medical Device Recall · September 9, 2025

  Draeger, Inc.

  Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetiz

  The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

  Class I

• Medical Device Recall · September 9, 2025

  Biomet, Inc.

  Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

  The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.

  Class II

• Food Recall · September 9, 2025

  Eden¿¿¿s Elixirs, LLC

  Eskay Brands Mint flavored tablets. 40mg 7OH/550mg Tablet- Eskay Brands-Mint, Chewable tablet, no shelf-life. Dosage: 2 doses per tablet. 10,000 or less per bulk bag. Bulk package and is not sold dire

  Undeclared Yellow #5

  Class II

• Medical Device Recall · September 9, 2025

  Draeger, Inc.

  Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthet

  The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

  Class I

• Medical Device Recall · September 9, 2025

  BioPro, Inc.

  BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH LT 14090 HEAD FEMORAL 28 MD LT 14091 HEAD FEMORAL 28 LG LT 14094 HEAD FEMORAL 32 SH LT 14095 HEAD FEMORAL 32 MD LT 14096 H

  Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

  Class II

• Food Recall · September 9, 2025

  EUREKA INC

  Cinnamon, Clear Plastic Container, 100G, UPC 6251136 034139

  Elevated levels of lead.

  Class II