Safety Recalls

15,200 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 4,451–4,500 of 15,200

• 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

  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

• Food Recall · September 11, 2025

  TROPICANA BRANDS GROUP

  Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening

  A manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability.

  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

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180

  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

  Boston Scientific Corporation

  CX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404430 (12CM PS IZ), (2) 72404431 (15CM PS IZ), (3) 72404432 (18CM PS IZ), (4) 72404433 (21CM PS IZ), (5) 72404434 (24CM PS IZ), (6)

  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

  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 II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180

  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

  CareFusion 303, Inc.

  BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron Filter, SmartSite Y-Site 10015414, 180 Micron Filter 2447-0007, Ball Valve S

  Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.

  Class I

• 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

  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

  Boston Scientific Corporation

  CXR Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404461 (12CM PS IZ), (2) 72404462 (14CM PS IZ), (3) 72404463 (16CM PS IZ), (4) 72404464 (18CM PS IZ), (5) 72404465 (10CM IP IZ), (6)

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

  Class II

• Food Recall · September 11, 2025

  Harris Teeter

  Harris Teeter CINNAMON TEXAS TOAST, NET WT 5.0oz (0.31g), INGREDIENTS BREAD*** CONTAINS WHEAT, UPC 0 72036 95734 4, 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

  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

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180

  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

  OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40

  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

  OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60

  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

  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

  Boston Scientific Corporation

  LGX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404450 (12CM PS IZ), (2) 72404451 (15CM PS IZ), (3) 72404452 (18CM PS IZ), (4) 72404453 (21CM PS IZ), (5) 72404455 (12CM IP IZ), (6)

  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

  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

• Medical Device Recall · September 11, 2025

  Boston Scientific Corporation

  TENACIO Pump without InhibiZone; UPN: 72404420;

  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 MP60

  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

  Boston Scientific Corporation

  LGX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404405 (12CM IP), (2) 72404407 (18CM 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

  BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150

  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

  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

  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

• 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

• Consumer Product Recall · September 11, 2025

  Epoca International LLC, of Boca Raton, Florida

  Paris Hilton Mini Beauty Fridges

  The recalled mini fridge's electrical switch can short circuit, causing it to overheat, posing a fire and burn hazard.

  Unclassified

• 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

• Medical Device Recall · September 11, 2025

  Medline Industries, LP

  Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush syringes

  Medline has identified a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.

  Class II

• Medical Device Recall · September 11, 2025

  Olympus Corporation of the Americas

  BRONCHOVIDEOSCOPE OLYMPUS BF-Q170

  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

  In My Jammers, of Gilbert, Arizona

  In My Jammers Button Up Flare Pajama Sets

  The recalled children's pajama sets violate mandatory standards for children's sleepwear flammability, posing a risk of burn injuries to children.

  Unclassified

• 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

• 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

  Ethicon Endo-Surgery Inc

  ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80

  The devices were shipped unsterilized.

  Class II

• 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

• 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

  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

  BRONCHOVIDEOSCOPE OLYMPUS BF-H1100

  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

• 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

• 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 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

• 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

• 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

  Vanilla Cookies with Raspberry Peach Jam

  Undeclared Red 3 and Blue 1

  Class II