The Recall Desk

State

Mississippi product recalls

72,940 recalls have nationwide distribution and so reach Mississippi. 5,349 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total
5,349
Critical
923
Severe
1,126
Most recent
2026-09-09

Of the 5,349 recalls naming Mississippi we have scored against our rubric, 923 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,126 (21%) are Severe.

These figures cover only the 5,349 recalls whose distribution notice names Mississippi specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4451–4475 of 78289

  • CriticalFDA (Devices)·Z-0445-2026·2025-11-19

    Airway procedure kits recalled over cracks in anesthesia circuit tubing

    Medline is recalling ENT and laryngoscopy-bronchoscopy kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; ENT DYNJ909128I; LARYNGOSCOPY - BRONCHOSCOPY DYNJ909114D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0442-2026·2025-11-19

    Adult anesthesia circuit kits recalled over cracked expandable tubing

    Medline is recalling multiple adult 120-inch expandable anesthesia circuits after complaints of leaks caused by cracks in the tubing. The FDA has classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers: ADULT 120 EXPANDABLE W/MASK DYNJAA10591; ANES CIRC 120IN EXP-LF DYNJAA6555G; ANES CIRCUIT ADULT 120"-LF DYNJAA10817; ANESTHESIA 120" ADLT-LF DYNJAA10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0447-2026·2025-11-19

    Surgical convenience kits recalled over cracked anesthesia circuit tubing

    Medline is recalling 96,406 breast and hernia convenience kits after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience Kit, BREAST HERNIA DYNJ909125G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0187-2026·2025-11-19

    Red Bali kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom Red Bali powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom Red Bali powder is packaged in seal mylar pouches: Monarch Premium Kratom Red Bali, 4oz powder (112g), UPC 851006008442 Monarch Premium Kratom Red Bali, 8oz powder (224g), UPC 706970483859 Monarch Premium Kratom Red Bali, 2oz powder (56g), UPC 8510060084
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0449-2026·2025-11-19

    Expandable anesthesia circuits recalled over cracks causing leaks in tubing

    Medline is recalling the 120-inch latex-free ExtendFlex anesthesia circuit after complaints of leaks caused by cracks in the expandable tubing. The FDA has classified it Class I.

    Product
    Anesthesia circuit kit; CIRCUIT,ANES,EXTENDFLEX,120,LF DYNJAA10230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0199-2026·2025-11-19

    Peach salsa recalled over Listeria in peaches from one supplier

    GBC Food Services is recalling 154.88 pounds of 14 oz peach salsa because the peaches supplied by Moonlight Peaches are potentially contaminated with Listeria. The FDA classified it Class I.

    Product
    Peach Salsa; UPC 85006540364 14oz (397g); Use by 10/12/2025 to 10/29/2025
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Devices)·Z-0434-2026·2025-11-19

    Detachable brain aneurysm coils recalled because they may fail to detach

    Cerenovus is recalling 12,004 CEREPAK Detachable Coil System units because the coils may fail to detach, which could result in hemorrhagic and ischemic stroke. The FDA classified it Class I.

    Product
    CEREPAK Detachable Coil System - Name/REF: UNIFORM 2MM X 2.5 CM/FCX100202, UNIFORM 2.5MM X 3.3 CM/FCX100253, UNIFORM 3MM X 5.4 CM/FCX100305, UNIFORM 3.5MM X 6.6 CM/FCX100356, UNIFORM 4MM X 7.5 CM/FCX100407, UNIFORM 4MM X 11.5 CM/FCX100412, UNIFORM 5MM X 9.7 CM/FCX100509, UNIFORM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0450-2026·2025-11-19

    Robotic surgery kits recalled over cracked anesthesia circuit tubing

    Medline is recalling GYN Robotic and Robotic Prostate convenience kits after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience kits; DYNJ901046M GYN ROBOTIC DYNJ909120D ROBOTIC PROSTATE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0451-2026·2025-11-19

    Orthopedic and spine kits recalled over cracked anesthesia circuit tubing

    Medline is recalling ortho spine, total joint and kyphoplasty convenience kits after complaints of anesthesia circuit leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience kits; DYNJ901047R ORTHO SPINE FUMICH DYNJ902308K TOTAL JOINT DYNJ909111F DR SALMA'S SPINE DYNJ909117G PATTERSON TOTAL JOINT DYNJ909113F KYPHOPLASTY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0446-2026·2025-11-19

    Laparoscopy and cysto kits recalled over cracked anesthesia circuit tubing

    Medline is recalling robotic gastric sleeve, cysto and general laparoscopy kits after complaints of anesthesia circuit leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D GENERAL LAPAROSCOPY-LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0185-2026·2025-11-19

    Bali Gold kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom Bali Gold powder in 4 oz and 8 oz sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom Bali Gold powder is packaged in seal mylar pouches: Monarch Premium Kratom Bali Gold, 4oz powder (112g), UPC 851006008428 Monarch Premium Kratom Bali Gold, 8oz powder (224g), UPC 706970483712
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0444-2026·2025-11-19

    Open heart and vascular kits recalled over cracked anesthesia circuit tubing

    Medline is recalling open heart supplement and vascular kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0188-2026·2025-11-19

    White Elephant kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom White Elephant powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom White Elephant powder is packaged in seal mylar pouches: Monarch Premium Kratom, White Elephant, 4oz powder (112g), UPC 851006008480 Monarch Premium Kratom, White Elephant, 0.5oz powder (14g), UPC 851006008756 Monarch Premium Kratom, White Elephant, 8oz p
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0186-2026·2025-11-19

    Green Maeng Da kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom Green Maeng Da powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom Green Maeng Da powder is packaged in seal mylar pouches: Monarch Premium Kratom Green Maeng Da, 4oz powder (112g), UPC 851006008466 Monarch Premium Kratom Green Maeng Da, 0.5oz powder (14g), UPC 851006008770 Monarch Premium Kratom Green Maeng Da, 2
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0443-2026·2025-11-19

    Breathing kits recalled over cracks in the expandable anesthesia tubing

    Medline is recalling the latex-free Breathing Kit DYNJ10550 after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; BREATHING KIT-LF DYNJ10550
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0448-2026·2025-11-19

    Urology and hip pinning kits recalled over cracked anesthesia circuit tubing

    Medline is recalling ortho spine, urology minor, set up and hip pinning convenience kits after complaints of anesthesia circuit leaks from cracked tubing. The FDA classified it Class I.

    Product
    Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR DYNJ909132F SET UP DYNJ909308D HIP PINNING
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V800000·2025-11-19

    McNeilus Recalls 2024-2025 Volterra ZSL Trucks Due to Software Error

    McNeilus is recalling 2024-2025 Volterra ZSL side loader garbage trucks because a software error may cause grabber fingers to move without operator input, posing a risk of injury or crash.

    Product
    MCNEILUS — MCNEILUS VOLTERRA ZSL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0454-2026·2025-11-19

    CARESCAPE ONE monitors recalled over batteries that fail to hold charge

    GE Healthcare is recalling 5,935 CARESCAPE ONE patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.

    Product
    CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0471-2026·2025-11-19

    Five millimetre blunt tip sealers recalled over trapped residual material

    Medline is recalling two reprocessed LigaSure Blunt Tip sealer/dividers, 5 mm x 37 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal LigaSure Blunt Tip Sealer/Divider, Compatible with FT10 Generator, 5 mm x 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0183-2026·2025-11-19

    Tense-X supplement recalled because it contains magnesium salicylate

    Professional Botanicals is recalling 253 bottles of Tense-X capsules because the product contains magnesium salicylate.

    Product
    Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0497-2026·2025-11-19

    Larger bore nasal feeding tubes recalled for possible occlusion

    Applied Medical Technology is recalling NutraGlide 6 F-8 F x 55 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.

    Product
    Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-I
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0182-2026·2025-11-19

    Dietary supplement recalled because it contains magnesium salicylate

    Professional Botanicals is recalling 430 bottles of Total Comfort capsules because the product contains magnesium salicylate.

    Product
    Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sku: PB173.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0490-2026·2025-11-19

    Reprocessed ultrasonic shears recalled because they may stick in the on position

    Stryker Sustainability Solutions is recalling 22,476 reprocessed HARMONIC FOCUS shears because a manufacturing issue may leave them stuck in the on position, causing continuous activation.

    Product
    HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STERILEEO, RX ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0483-2026·2025-11-19

    Fifteen millimetre snares recalled over holes compromising package sterility

    Olympus is recalling 18,174 Single Use Electrosurgical Snares SD-400U-15 because sterility may be compromised by small holes formed during packaging or transportation.

    Product
    Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and
    Category
    Medical Device
    Distribution
    Distributed nationwide