The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

14326–14350 of 22168

  • HighFDA (Drugs)·D-1102-2023·2023-08-30

    Lugol's Strong Iodine Solution Recalled Due to Manufacturing Quality Deviations

    Ecometics, Inc. is recalling Lugol's Strong Iodine Solution nationwide due to manufacturing quality deviations. Consumers with affected prescription vials should consult their healthcare provider.

    Product
    Lugol's (Strong Iodine Solution USP), Each mL contains Iodine 0.05gm and potassium iodide 0.100gm, 8mL Single Use Vials, Rx Only, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6064-0, Ref 6064.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·23785·2023-08-24

    Ecnup Kids Bike Helmets Recalled Due to Head Injury Risk

    Ecnup kids bike helmets sold on Amazon do not meet federal safety standards for coverage, stability, and labeling. The helmets can fail to protect the head in a crash.

    Product
    Kids bike helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23784·2023-08-24

    Aiper Elite Pro Robotic Pool Vacuum Cleaners Recalled for Burn and Fire Hazards

    About 22,000 Aiper Elite Pro GS100 robotic pool vacuum cleaners are being recalled because the battery can overheat and catch fire when the charging cord is plugged in without the adapter. The manufacturer is replacing all recalled units with a different model.

    Product
    Aiper Elite Pro GS100 cordless robotic pool vacuum cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1427-2023·2023-08-23

    Romaine Lettuce Recalled Due to Deer Feces Contamination

    G.O. Corporation is recalling Romaine Lettuce 80/20 GB due to potential contamination with deer feces. The affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lettuce Romaine 80/20 GB, packaged in the following sizes and configurations: 1. Produce Code 448007, 2-5 lb. bags per shipping case, 2. Produce Code 448007, 4-5 lb. bags per shipping case, 3. Produce Code 448110, 4-5 lb. bags per shipping case.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1431-2023·2023-08-23

    NatureBest Pre-Cut Lettuce Kits Recalled for Potential Deer Fecal Contamination

    NatureBest Pre-Cut & Produce LLC is recalling salad kits sold in Texas due to potential presence of deer fecal matter. No illnesses have been reported.

    Product
    SALAD KIT-NO COLOR-11CT LETTUCE-4 WAY/MIX-4/5# LETTUCE-ROM/GRN LF 60/40-4/3# LETTUCE-ROMAINE-SHREDDED-4/5# LETTUCE-ROM-1x1-GRN ONLY-6/2# LETTUCE-4 WAY/MIX-2/5# LETTUCE-4 WAY/MIX-1/5# LETTUCE-ROMAINE-CUT-6/2#
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2424-2023·2023-08-23

    Endoscopic surgical grasper recalled due to rotation knob defect

    Carefusion is recalling specific lots of Snowden-Pencer Diamond-Touch endoscopic graspers due to a manufacturing defect that may cause the rotation knob to crack or break. Affected units were distributed in the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI 5MM, 32CM, RATCHETED HANDLE, REF SP90-7066; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1442-2023·2023-08-23

    Uro Kid Support Capsules recalled due to potential E. coli contamination

    Global Vitality Inc. is recalling Uro Kid Support Capsules due to potential E. coli contamination. The affected product was distributed to a single location in California.

    Product
    Food Research International - Uro Kid Support Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2417-2023·2023-08-23

    Endoscopic surgical graspers recalled for potential rotation knob cracking

    Carefusion is recalling Snowden-Pencer MIS surgical graspers (lot B23) distributed in the US and Canada because the rotation knob may crack or break due to a manufacturing adhesive defect. Affected devices could malfunction during surgical use.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7020; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2427-2023·2023-08-23

    Endoscopic surgical clamp recalled for potential rotation knob failure

    Carefusion recalls Snowden-Pencer MIS Diamond-Touch Clamps (Lot B23) due to potential cracking of the rotation knob from incorrect adhesive use. The 7 affected units were distributed to the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 45CM, RATCHETED, REF SP90-7243; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2414-2023·2023-08-23

    FreeStyle Libre 2 Readers may fail to activate new sensors

    FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.

    Product
    FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2421-2023·2023-08-23

    Surgical Clamp Recall: Rotation Knob May Crack or Break

    Snowden-Pencer endoscopic surgical clamps may have rotation knobs that crack or break due to manufacturing defect. Lot B23 units should not be used.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 50 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7045; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2419-2023·2023-08-23

    Surgical clamp rotation knob may crack or break due to manufacturing defect

    Specific lots of Snowden-Pencer surgical clamps may have rotation knobs that crack or break due to incorrect adhesive use in manufacturing. Eight units with lot numbers L22, B23, or C23 distributed in the US and Canada are affected.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7043; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2405-2023·2023-08-23

    Hip Screw Labeled as Wrong Size: 30mm Screws Mislabeled as 25mm

    Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.

    Product
    CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2422-2023·2023-08-23

    Endoscopic Surgical Clamp Recalled Due to Potential Rotation Knob Failure

    Carefusion is recalling specific lots of Snowden-Pencer MIS endoscopic surgical clamps due to potential cracking or breaking of the rotation knob caused by incorrect adhesive use during manufacturing.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7046; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1432-2023·2023-08-23

    Garden Cut Romaine Lettuce Recalled for Potential Deer Feces Contamination

    Get Fresh Produce is recalling Garden Cut Romaine lettuce (product 9386) because it may be contaminated with deer feces. The recall affects 1,404 pounds distributed in Illinois and Florida.

    Product
    Garden Cut Romaine 1x1 Chopped 6/2 LB (product number 9386) packed in corrugated boxes with an inner plastic bag (6, 2lb bags per case)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1433-2023·2023-08-23

    Garden Cut Lettuce Greek Mix Salad recalled for possible deer feces contamination

    Get Fresh Produce, Inc. is recalling Garden Cut Lettuce Greek Mix Salad (product number 10149) due to possible contamination with deer feces. Affected product was distributed in Illinois and Florida.

    Product
    Garden Cut Lettuce Greek Mix Salad (product number 10149) 10 LB packed in corrugated boxes with an inner plastic bag. Product consists of: 1"x1" Romaine, 1/8" red cabbage, and 1/8" green cabbage.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1434-2023·2023-08-23

    Benton's Snack Packs Recalled for Undeclared Peanut Allergen

    Benton's 100 Calorie Snack Packs are recalled because they contain undeclared peanut, a major allergen. Consumers with peanut allergies may experience severe reactions if they consume this product.

    Product
    Benton's 100 Calorie Snack Packs Baked Chocolate Wafer Snacks 6-0.81 OZ (23g) Packs Net Wt. 4.86 oz UPC: 4 099100 040416 Packaged in a paper carton, 16 cartons per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1435-2023·2023-08-23

    Annie's Homegrown Graham Snack Recalled for Undeclared Peanut

    Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla 6.75 oz boxes are recalled due to undeclared peanut. Consumers with peanut allergies should not consume this product.

    Product
    Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla Flavored With Other Natural Flavors Graham-Style Snacks Net Wt 6.75 oz (191g) UPC: 13562 00019 Packaged in cartons, 7 and 12 retails cartons per case
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1429-2023·2023-08-23

    Romaine Lettuce Recalled Due to Potential Deer Feces Contamination

    G.O. Corporation is recalling Romaine Lettuce All American sold in four states due to potential contamination with deer feces.

    Product
    Lettuce Romaine All American, packaged in the following sizes and configurations: 1. Produce Code 476702, 1-5 lb. bag per shipping case, Customer UPC 8398299; 2. Produce Code 476709, 4-5 lb. bags per shipping case, Customer UPC 476709, 8336156, and 8398281.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2416-2023·2023-08-23

    Endoscopic Grasper Instrument Recalled for Rotation Knob Failure Risk

    Carefusion 2200 Inc is recalling specific lots of the Snowden-Pencer DIAMOND-TOUCH GRASPER endoscopic surgical instrument due to a manufacturing defect that may cause the rotation knob to crack or break, potentially compromising surgical performance.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPER DIAMOND JAW BABCOCK 5MM, 32CM, RATCHETED, REF SP90-7018; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1402-2023·2023-08-23

    Trader Joe's Falafel Recalled for Foreign Object Contamination

    Trader Joe's Fully Cooked Falafel Heat & Eat is being recalled from Connecticut, Texas, and Illinois due to the presence of rocks in the product. Consumers should return affected packages to the point of purchase.

    Product
    Trader Joe's Fully Cooked Falafel Heat & Eat NET WT. 12 OZ (340g) Distributed and Sold Exclusively By: Trader Joe's Monrovia, CA 91016 UPC 0093 9355
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1425-2023·2023-08-23

    Romaine lettuce blend recalled for potential fecal contamination

    G.O. Corporation is recalling a lettuce blend product due to potential contamination with deer feces. Affected products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lett. Blend Rom/End/Rad-All Seasons packaged in the following sizes and configurations: 1. Produce Code 444032, 6-2 lb. bags per shipping case 2. Produce Code 444047, 3-2lb. bags per shipping case.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1436-2023·2023-08-23

    Gluten Free MI-DEL Swedish Style Ginger Snaps recalled for undeclared peanut

    Gluten Free MI-DEL Swedish Style Ginger Snaps (8 oz and 10 oz packages) are being recalled because they contain undeclared peanut. Consumers with peanut allergies should not consume this product and should return it to the retailer or dispose of it safely.

    Product
    Gluten Free MI-DEL Swedish Style Ginger Snaps Net Wt. 8 oz (227g) & 10 oz UPC:3068476890. Packaged in plastic bags, 12 bags per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1423-2023·2023-08-23

    Romaine lettuce recalled due to potential deer feces contamination

    G.O. Corporation is recalling romaine lettuce in multiple package sizes due to potential contamination with deer feces. The affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Romaine lettuce packaged into the following configurations and sizes: 1. Lettuce Romaine Shred, Produce Code 720325, 4-2.5lb. bags per shipping case, Customer UPC 9120457. 2. Romaine Shred 1/4", Produce Code 720425, 4-2.5lb bags per shipping case, Customer UPC 7641269 and
    Category
    Food
    Distribution
    4 states