The Recall Desk

Archive

October 2025 recalls

804 recalls were announced in October 2025.

What the numbers show

Critical
179
Severe
78
High
390
Moderate
154
Low
3

Of the 804 recalls this month scored against our rubric, 22% are Critical, 10% are Severe.

Which agencies issued them

101–200 of 804

  • HighFDA (Devices)·Z-0206-2026·2025-10-29

    ENFit sump tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14FR 48IN 8888264960E ENFit" Salem Sump" PVC Tube 16Fr 48IN 8888264986E ENFit" SA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0297-2026·2025-10-29

    Millenium gamma cameras recalled over risk of detector falling from mount

    GE HealthCare is recalling 1,386 Millenium MG/MC gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium MG/MC; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0083-2026·2025-10-29

    Jumbo meatball subs recalled over metal shavings in mozzarella ingredient

    MG Foods is recalling 117 Jumbo Meat Ball Subs because the mozzarella cheese ingredient has the potential to be contaminated with metal shavings.

    Product
    Jumbo Meat Ball Sub; Net Weight: 8.9oz; Product Code: Fresh Thru 10-15-25, 10/16/2025, 10/20/2025 In clear plastic packaging with white sticker label
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0233-2026·2025-10-29

    Oral thermometer probes recalled after being programmed with rectal configuration

    Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.

    Product
    Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0300-2026·2025-10-29

    Millenium MPS gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 54 Millenium MPS gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium MPS; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0302-2026·2025-10-29

    Sopha Medical Vision cameras recalled over risk of detector falling

    GE HealthCare is recalling 205 Sopha Medical Vision gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Sopha Medical Vision (SMV) DSXi/DST-XLi,/ DST-XL/ DSTi; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0298-2026·2025-10-29

    Millenium Myosight gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 82 Millenium Myosight gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium Myosight; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0108-2026·2025-10-29

    Sprite cans recalled over potential presence of metal foreign material

    Coca-Cola Southwest Beverages is recalling 791 units of Sprite 12 oz cans in Texas over the potential presence of metal foreign material.

    Product
    Sprite 12oz Can 35 pack 49000058482 / JUN2926MAA Sprite 12oz Can 12 pack 49000028928 / JUN2926MAA Sprite 12oz Can 12 pack 49000028928 / JUN3026MAB
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0036-2026·2025-10-29

    Ketorolac injection vials recalled after glass particulate found in product

    Aspiro Pharma is recalling Ketorolac Tromethamine Injection USP 60 mg/2 mL across several lots because of particulate matter identified as glass.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0140-2026·2025-10-29

    Shredded imitation crabmeat recalled over potential Clostridium botulinum from temperature abuse

    Ocean's Kitchen is recalling 496 cases of shredded imitation crabmeat for potential contamination with Clostridium botulinum due to a risk of temperature abuse during chilled storage at the firm.

    Product
    Oceans Kitchen IMITATION CRABMEAT SHREDDED Made From Wild Fish, Refrigerated, vacuum package. Net wt. per bag 2.5 lbs. UPC 1 90456 75654 2. These 2.5lb. bags are not for retail sales. Each master case contains 12/2.5lbs. bags. Net wt. per case: 30lbs. UPC 14972195756549. Oceans
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0209-2026·2025-10-29

    Gastric sump anti-reflux valves recalled after breakage complaints from excessive force

    Cardinal Health is recalling all lots of Salem Sump Anti-Reflux Valves after complaints of valve breakage due to excessive force during use, and is providing additional guidance for use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem Sump" Anti-Reflux Valve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0232-2026·2025-10-29

    Insulin pumps recalled over software defect causing unexpected correction bolus

    Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.

    Product
    t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0237-2026·2025-10-29

    Blood culture systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 1,086 BD BACTEC Blood Culture Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. INSTRUMENT BACTEC 9120 UNREPAIRED, Catalog Number: 44557008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0092-2026·2025-10-29

    Chocolate covered freeze-dried strawberries recalled over potential metal in product

    Georgia Nut Co is recalling 170,993 cases of tru fru Dark + White Chocolate Freeze-Dried Strawberries because of the potential for metal in the product.

    Product
    tru fru Dark + White Chocolate Freeze-Dried Strawberries. 1.7oz retail pouch UPC 850048358331. 12 retail units per case. 3.4oz retail pouch UPC 850048358270. 6 retail units per case. 13oz retail pouch UPC 850048358379. 16 retail units per case.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0234-2026·2025-10-29

    Prefilled saline flush syringes recalled over sodium chloride concentration shortfall

    Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.

    Product
    Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush syringes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0288-2026·2025-10-29

    Defibrillator pad packs recalled over damaged pins disrupting electrical contact

    HeartSine Technologies is recalling 1,291,165 Pad-Pak units because defibrillator pads may contain damaged pins that disrupt the mechanical fit and electrical contact.

    Product
    HeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03, PAD-PAK-04, PAD-PAK-07, PAD-PAK-03J, PAD-PAK-04J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0110-2026·2025-10-29

    Frozen organic chopped spinach recalled over potential Listeria monocytogenes contamination

    Del Mar Food Products is recalling 966 cases of Organic IQF Chopped Spinach in 35 lb packs for potential contamination with Listeria monocytogenes.

    Product
    ORGANIC IQF CHOPPED SPINACH 35 lbs. Net Weight Product is not ready to eat. For food safety, cook to an internal temperature of 165 degrees F as measured with a food thermometer. PACKED BY DEL MAR FOOD PRODUCTS CORP., WATSONVILLE, CA 95077, U.S.A. UPC: 1822V
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0227-2026·2025-10-29

    Bipolar hip heads recalled downstream after femoral components failed transit testing

    Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.

    Product
    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 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Asse
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0109-2026·2025-10-29

    Frozen organic spinach recalled over potential Listeria monocytogenes contamination

    Sno Pac Foods is recalling 4,006 cases of Frozen Organic Spinach in 10 oz poly bags because the spinach has the potential to be contaminated with Listeria monocytogenes.

    Product
    Frozen Organic Spinach Net Wt. 10 oz (283.5g) poly bags packaged under the following brands: 1. Sno Pac Frozen Vegetables, UPC 0 24284-96910 5. Keep Frozen. Packed and Distributed by: Sno Pac Foods, Inc., 521 West Enterprise, Caladonia, MN 55921. 2. ***This product di
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·H-0127-2026·2025-10-29

    Dubai style chocolate recalled because wheat is not declared as allergen

    Rolling Pin Baking Company is recalling 127,680 units of Rolling Pin Dubai Style Chocolate because the product does not declare wheat in the allergen statement.

    Product
    Rolling Pin brand Dubai Style Chocolate; 17.64 oz stand up pouch; Ingredients: Sugar, Cocoa Butter, Vegetable Fats, Whole Milk Powder, Pistachio (Tree Nut), Skimmed Milk Powder, Cocoa Mass, Kunefa, Soy Lecithin, Natural Vanilla Powder; Allergens: Contains Milk, Soy, Nuts (Pistach
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-0299-2026·2025-10-29

    Millenium MPR gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 292 Millenium MPR gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium MPR; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0236-2026·2025-10-29

    BACTEC FX instruments recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 177 BD BACTEC Blood Culture System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument Top Remanufactured Bactec Fx, Catalog Number: 441676. 3. BACTEC 9240 System, Catalog Number: 445569. 4. BD BACTEC FX40 Instrum
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0214-2026·2025-10-29

    Central monitoring stations recalled over reboot loop at specific network sizes

    GE HealthCare is recalling 2,306 Carescape Central Stations running software V3.0.5 because the system can enter a continuous reboot cycle, losing central monitoring of connected patients.

    Product
    GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5, Part Number 5867474-03; Medical Display, cathode ray tube
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0212-2026·2025-10-29

    AC joint fixation implants recalled over potentially missing slotted button assembly

    Biomet is recalling 98 ZipTight Acute AC Joint Implants from one lot because of the potential for a missing slotted button assembly.

    Product
    BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0208-2026·2025-10-29

    Silicone stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0112-2026·2025-10-29

    Frozen cooked shrimp recalled across four brands over cesium 137 contamination

    Southwind Foods is recalling frozen cooked shrimp under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736
    Category
    Food
    Distribution
    34 states
  • ModerateFDA (Devices)·Z-0257-2026·2025-10-29

    Canon ready 40KW systems recalled with reminder about improper cleaning

    Sedecal is recalling six SM-40HF-B-D-C 40KW Canon Ready mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model SM-40HF-B-D-C; 40KW - CANON READY, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0254-2026·2025-10-29

    Battery powered mobile X-ray unit recalled with water resistance reminder

    Sedecal is recalling one SM-20HF-Batt 20KW analog mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-20HF-Batt; 20KW ANALOG, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0242-2026·2025-10-29

    Digital diagnostic X-ray systems recalled with reminder about improper cleaning

    Sedecal is recalling 56 SM-40HF-B-D-KM (AeroDR X30) mobile digital diagnostic X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Sedecal Mobile Digital Diagnostic X-Ray Systems; SM-40HF-B-D-KM (AeroDR X30)
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0221-2026·2025-10-29

    uCT ATLAS scanners recalled because third party covers can jam table

    UIH Technologies is recalling two uCT ATLAS computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT ATLAS MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0282-2026·2025-10-29

    SED URS LP X-ray system recalled with water resistance reminder

    Sedecal is recalling the SED URS LP mobile X-ray system, serial 40116, after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    SED URS LP, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0222-2026·2025-10-29

    PET CT systems recalled because third party covers can trap during movement

    UIH Technologies is recalling two uEXPLORER PET/CT systems because third-party outer covers can become trapped between the patient table and gantry, causing mechanical interference.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uEXPLORER MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0263-2026·2025-10-29

    Four 40KW 50C X-ray systems recalled with water resistance reminder

    Sedecal is recalling four SM-40HF-B-D-C 40KW 50C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 50C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0251-2026·2025-10-29

    Twelve mobile X-ray units recalled with reminder about water resistance limits

    Sedecal is recalling 12 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant and must be cleaned strictly per the manual.

    Product
    Model Number 40KWFXPLUS-710CW, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0259-2026·2025-10-29

    Another 40KW 55C X-ray unit recalled with water resistance reminder

    Sedecal is recalling one SM-40HF-B-D-C 40KW 55C mobile X-ray system, serial G37528, after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 55C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0273-2026·2025-10-29

    Mobile X-ray systems recalled with cleaning reminder over water resistance limits

    Sedecal is recalling 10 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant and must be cleaned strictly per the manual.

    Product
    Model Number SM-40HF-B-D-C; 40KW 70C READY, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0264-2026·2025-10-29

    Twenty seven 40KW 50G X-ray systems recalled with cleaning reminder

    Sedecal is recalling 27 SM-40HF-B-D-C 40KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 50G, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0249-2026·2025-10-29

    Twelve 40KWFXPLUS X-ray systems recalled with strict cleaning reminder

    Sedecal is recalling 12 model 40KWFXPLUS.005 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number 40KWFXPLUS.005, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0278-2026·2025-10-29

    Six 40KW mobile X-ray units recalled with strict cleaning reminder

    Sedecal is recalling six SM-40HF-B-D-C 40KW.002 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW.002, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0218-2026·2025-10-29

    uCT 550 scanners recalled because third party covers can jam table

    UIH Technologies is recalling 22 uCT 550 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT 550 MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0229-2026·2025-10-29

    Locking bone screws recalled after packaging labeled with the wrong length

    Synthes is recalling 122 low profile locking screws because 42mm screws were packaged and labeled as 46mm and 46mm screws were labeled as 42mm, though the etched length is correct.

    Product
    LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 42MM / XL25/ STER. Product Code: 04.045.342TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0277-2026·2025-10-29

    One hundred forty two 40KW X-ray systems recalled with cleaning reminder

    Sedecal is recalling 142 SM-40HF-B-D-C 40KW mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0271-2026·2025-10-29

    One hundred eighty one 40KW 70C X-ray systems recalled with cleaning reminder

    Sedecal is recalling 181 SM-40HF-B-D-C 40KW 70C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 70C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0031-2026·2025-10-29

    Gabapentin blister packs recalled after unknown impurity exceeded specification

    The Harvard Drug Group is recalling Gabapentin Capsules USP 100 mg in 10-capsule blister packs after routine stability testing returned an out-of-specification result for highest unknown impurity.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0230-2026·2025-10-29

    Foot plating systems recalled to remove a sterilization option from instructions

    CPM Medical Consultants is updating the Fuse ULTRA Foot Plating System instructions for use to remove a sterilization option that does not apply in the United States.

    Product
    Fuse ULTRA Foot Plating System Instructions for Use. Models: OS200400, OS200401, OS328017, OS200020L, OS200025L, OS200120L, OS200125, OS200125L, OS200135, OS200324, OS200325, OS200326, OS328026, OS328028C, OS216150, OS218150, OS292110, OS292120, OS292160, OS292200, OS200516, O
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0260-2026·2025-10-29

    Fourteen 40KW 70C X-ray systems recalled with strict cleaning reminder

    Sedecal is recalling 14 SM-40HF-B-D-C 40KW 70C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model SM-40HF-B-D-C; 40KW 70C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0223-2026·2025-10-29

    uMI 550 PET systems recalled because third party covers can jam

    UIH Technologies is recalling 95 uMI 550 PET/CT systems because third-party outer covers can become trapped between the patient table and gantry.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uMI 550 MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0224-2026·2025-10-29

    uMI 780 PET systems recalled because third party covers can jam

    UIH Technologies is recalling three uMI 780 PET/CT systems because third-party outer covers can become trapped between the patient table and gantry.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uMI 780 MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0095-2026·2025-10-29

    Zicam fruit drops recalled because label omitted elderberry as an ingredient

    Church & Dwight is recalling 21,912 bottles of Zicam Medicated Fruit Drops Elderberry Flavor because the label failed to list elderberry as an ingredient.

    Product
    ZICAM COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY — ZICAM COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY (ZINC ACETATE ANHYDROUS, ZINC GLUCONATE, AND SAMBUCUS NIGRA FLOWERING TOP)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0033-2026·2025-10-29

    Cetirizine tablets recalled because tablets were imprinted with the wrong identifier

    JB Chemicals is recalling 13,440 bottles of Cetirizine Hydrochloride Tablets USP 10 mg because the tablets were imprinted with the wrong identification code.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0032-2026·2025-10-29

    Cetirizine hundred count bottles recalled over tablets imprinted with wrong identifier

    JB Chemicals is recalling 9,936 hundred-count bottles of Cetirizine Hydrochloride Tablets USP 10 mg because the tablets were imprinted with the wrong identification code.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0228-2026·2025-10-29

    Forty six millimetre locking screws recalled over wrong length on packaging

    Synthes is recalling 120 low profile locking screws because 42mm screws were packaged and labeled as 46mm and 46mm screws were labeled as 42mm, though the etched length is correct.

    Product
    LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 46MM / XL25/ STER. Product Code: 04.045.346TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0275-2026·2025-10-29

    Canon ready X-ray unit recalled with water resistance cleaning reminder

    Sedecal is recalling one SM-40HF-B-D-C 40KW Canon Ready mobile X-ray system, serial G41234, after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW CANON READY, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0225-2026·2025-10-29

    uMI Panorama PET systems recalled because third party covers can jam

    UIH Technologies is recalling four uMI Panorama 35 PET/CT systems because third-party outer covers can become trapped between the patient table and gantry.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uMI Panorama 35 MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0266-2026·2025-10-29

    Mobile X-ray system recalled with reminder that unit is not waterproof

    Sedecal is recalling one SM-40HF-B-D-C 40KW 55C/60C mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 55C/60C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0219-2026·2025-10-29

    CT scanners recalled because third party covers can jam table movement

    UIH Technologies is recalling 11 uCT 760 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT 760 MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0256-2026·2025-10-29

    Battery analog 32KW X-ray systems recalled with water resistance reminder

    Sedecal is recalling 22 SM-32HF-Batt 32KW analog mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model SM-32HF-Batt; 32KW ANALOG, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0261-2026·2025-10-29

    Battery analog 40KW X-ray systems recalled with water resistance reminder

    Sedecal is recalling nine SM-40HF-Batt 40KW analog mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-Batt; 40KW ANALOG, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0034-2026·2025-10-29

    Olopatadine eye drops recalled after unspecified impurity exceeded specification limit

    USV Private Limited is recalling 8,952 bottles of Olopatadine Hydrochloride Ophthalmic Solution USP 0.1% after an unspecified impurity exceeded the specification limit.

    Product
    Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 %, 5 mL (0.17 FL OZ) bottles, Manufactured for: SOLA PHARMACEUTICALS LLC, Baton Rouge, LA 70810, NDC 70512-0520-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0279-2026·2025-10-29

    Six 40KW mobile X-ray systems recalled with cleaning instruction reminder

    Sedecal is recalling six SM-40HF-B-D-C 40KW.005 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW.005, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0280-2026·2025-10-29

    Six demo mobile X-ray systems recalled with strict cleaning reminder

    Sedecal is recalling six 40KW70CDEMO.005 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW70CDEMO.005, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0270-2026·2025-10-29

    Four 40KW 55C X-ray systems recalled with water resistance reminder

    Sedecal is recalling four SM-40HF-B-D-C 40KW 55C/60C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 55C/60C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0267-2026·2025-10-29

    Forty kilowatt 55G X-ray systems recalled with water resistance reminder

    Sedecal is recalling five SM-40HF-B-D-C 40KW 55G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 55G, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0268-2026·2025-10-29

    Two 40KW 55G X-ray systems recalled with water resistance reminder

    Sedecal is recalling two SM-40HF-B-D-C 40KW 55G/60G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 55G/60G, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0272-2026·2025-10-29

    Single 40KW 70C X-ray system recalled with water resistance reminder

    Sedecal is recalling one SM-40HF-B-D-C 40KW 70C EN mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 70C EN, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0037-2026·2025-10-29

    Bupropion extended release tablets recalled after failing tablet specifications

    Graviti Pharmaceuticals is recalling 46,512 bottles of Bupropion Hydrochloride Extended-Release Tablets USP (XL) 300 mg from one batch for failed tablet specifications.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0276-2026·2025-10-29

    Canon ready mobile X-ray system recalled with water resistance reminder

    Sedecal is recalling one SM-40HF-B-D-C 40KW Canon Ready mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW CANON READY.005, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0262-2026·2025-10-29

    Easy Moving Plus X-ray systems recalled with water resistance reminder

    Sedecal is recalling eight Easy Moving Plus SM-50HF-B-D-C 50KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Sedecal Easy Moving Plus Model Number SM-50HF-B-D-C; 50KW 50G, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0220-2026·2025-10-29

    uCT 780 scanners recalled because third party covers can jam table

    UIH Technologies is recalling two uCT 780 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT 780 MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0217-2026·2025-10-29

    uCT 530 scanners recalled because third party covers can jam table

    UIH Technologies is recalling eight uCT 530 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT 530 MD, Rx Only
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0098-2026·2025-10-29

    Motion sickness patches recalled for being marketed without approved application

    ibspot is recalling three boxes of Taoscare Motion Sickness Patches because the product was marketed without an approved new drug application.

    Product
    Taoscare Motion Sickness Patches 36-count box, Henan Xinyongtal Medical Technology., Ltd., Address: he nan sheng zhou kou shi huai yang xian gong ye yuan qu, X003SR097N
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0258-2026·2025-10-29

    Thirty nine 40KW 50G X-ray systems recalled with cleaning reminder

    Sedecal is recalling 39 SM-40HF-B-D-C 40KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 50G, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0269-2026·2025-10-29

    Single 40KW 55C X-ray system recalled with water resistance reminder

    Sedecal is recalling one SM-40HF-B-D-C 40KW 55C mobile X-ray system, serial G37587, after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 55C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0285-2026·2025-10-29

    Three VIR3 mobile X-ray systems recalled with water resistance reminder

    Sedecal is recalling three SM_40HF_B_D_VIR3.004 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    SM_40HF_B_D_VIR3.004, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0255-2026·2025-10-29

    Thirty two kilowatt X-ray systems recalled with strict cleaning reminder

    Sedecal is recalling eight SM-32HF-B-D-C 32KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-32HF-B-D-C; 32KW 50G, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • LowFDA (Devices)·Z-0226-2026·2025-10-29

    Sterile blood lancets recalled over incorrect or missing device identifier codes

    Home Health US is recalling 4,661 One Step Sterile Lancets because of incorrect or missing Unique Device Identifier codes.

    Product
    One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 30g 06949517008854 28g 06949517008847 23g The Lancing System is intended for the hygienic collection of capillary blood for testing purposes from the side of a fingertip and from alternative sites, such
    Category
    Medical Device
    Distribution
    10 states
  • ModerateNHTSA·25V736000·2025-10-28

    Jayco motorhome certification labels may reverse front and rear axle data

    Jayco is recalling certain 2025-2026 Entegra Condor and Jayco Granite Ridge motorhomes because the certification label may have the front and rear axle information reversed.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, GRANITE RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·035-2025·2025-10-27

    E.A. Sween Recalls Pulled Pork Sandwiches Due to Plastic Contamination

    E.A. Sween Company is recalling approximately 127,887 pounds of pulled pork sandwiches that may contain pieces of plastic. The products were distributed nationwide.

    Product
    E.A. Sween Company — E.A. Sween Company Recalls Pulled Pork Sandwich Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V735000·2025-10-27

    Tesla Cybertruck accessory light bar can loosen from the windshield

    Tesla is recalling certain 2024 Cybertruck vehicles fitted with a service-installed off-road light bar because an incorrect surface primer may allow the light bar to loosen and detach.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·034-2025·2025-10-25

    Hormel Foods recalls frozen ready-to-eat chicken for metal contamination

    Hormel Foods is recalling about 4.8 million pounds of frozen ready-to-eat chicken products that may contain metal pieces.

    Product
    Hormel Foods Corporation — Hormel Foods Corporation Recalls Ready-To-Eat Frozen Chicken Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·033-2025·2025-10-24

    LSI, Inc. Recalls BBQ Pork Jerky Due to Possible Metal Contamination

    LSI, Inc. is recalling BBQ pork jerky because pieces of metal were found in the product. No injuries have been reported, but consumers should not eat the product.

    Product
    LSI, Inc. — LSI, Inc. Recalls BBQ Pork Jerky Product Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide

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