The Recall Desk

State

Delaware product recalls

73,576 recalls have nationwide distribution and so reach Delaware. 3,438 additional recalls listed Delaware specifically in their distribution scope.

What the numbers show

Total
3,438
Critical
477
Severe
1,110
Most recent
2026-10-14

Of the 3,438 recalls naming Delaware we have scored against our rubric, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,110 (32%) are Severe.

Which agencies issued them

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27651–27675 of 77014

  • ModerateFDA (Devices)·Z-0842-2021·2021-01-20

    Ansh Labs Recalls SARS-CoV-2 IgM ELISA Kits for Labeling Update

    Ansh Labs is recalling 327 SARS-CoV-2 IgM ELISA kits to update instructions and reduce the risk of false test results.

    Product
    AnshLabs - SARS-CoV2 IgM ELISA (u-Capture), IVD, REF: AL-1002, kit contents, Ab PLATE 1 X ! Plate, IgM Sample DIL 1 x 100 mL, ENZ CONJ CONC 1 x 1.5 mL, Calibrators A-C 3 x 1.2 mL, CONJ DIL 1 X 12 mL, Stop SOLN 1 X 12 mL, TMB SOLN 1 X 12 mL, WASH CONC A 1 X 60 mL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0830-2021·2021-01-20

    Steris Recalls Medisafe Distal Duck Kits Due to Bacteria Presence

    Steris is recalling specific lots of Medisafe Distal Duck Kits and Bags because they may contain Pseudomonas fluorescens bacteria. The agency notes there is no risk to patients.

    Product
    Medisafe Distal Duck Kit and Duck Bag, Cleaner, ultrasonic, medical instrument - Product Usage: intended to keep instruments moist during transportation between point of use and cleaning as an initial step of reprocessing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0824-2021·2021-01-20

    Fresenius NaturaLyte Liquid Acid Concentrate Drums Recalled for Low Levels

    Fresenius Medical Care is recalling 27 drums of NaturaLyte Liquid Acid concentrate because sodium and/or calcium levels were below manufacturing specifications.

    Product
    NaturaLyte Liquid Acid concentrate drums, Model Number 13-2201-5 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0228-2021·2021-01-20

    Precision Dose Recalls Chlorhexidine Gluconate Oral Rinse Due to cGMP Deviations

    Precision Dose Inc. is recalling Chlorhexidine Gluconate Oral Rinse USP 0.12% unit dose cups due to current Good Manufacturing Practice (cGMP) deviations.

    Product
    Chlorhexidine Gluconate Oral Rinse USP 0.12%, packaged in a) 15 mL x 30 Unit Dose Cups (30-pack case) NDC 68094-028-61, b) 15 mL x 100 Unit Dose Cups (100-pack case) NDC 68094-028-62, Rx only, Precision Dose, Inc., South Beloit, IL 61080.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0814-2021·2021-01-20

    Fresenius NaturaLyte Liquid Acid Concentrate Recall for Low Sodium Levels

    Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.

    Product
    NaturaLyte Liquid Acid concentrate bottles, Model Number 08-2231-2 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0808-2021·2021-01-20

    Clerio Vision Contact Lenses Recalled for Incorrect Power Labeling

    Clerio Vision is recalling one lot of contact lenses because the packaging labeled them as -2.25 power, but the lenses inside are -3.75 power.

    Product
    Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6 count) and UPC 675506804478 (12 count) - Product Usage: for daily wear is indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0221-2021·2021-01-20

    Akorn Recalls Levetiracetam Oral Solution Due to Leaking Bottles

    Akorn, Inc. is recalling specific lots of Levetiracetam Oral Solution because customer complaints reported the liquid leaking from the bottles.

    Product
    Levetiracetam Oral Solution, 100 mg/mL, 16 fl oz (473 mL) bottle, Rx Only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701; NDC 50383-241-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0771-2021·2021-01-20

    Siemens SOMATOM CT Scanner Software Recall for Scan Parameter Issues

    Siemens is recalling specific SOMATOM CT scanner systems due to a software issue that may prevent scan cancellation and reloading, potentially delaying diagnosis or requiring patient rescans.

    Product
    SOMATOM Force, Definition AS, Definition Edge, Definition Flash, Drive, Confidence and Edge Plus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0807-2021·2021-01-20

    Baxter Recalls VERITAS Collagen Matrix Patches Due to Undersized Width

    Baxter Healthcare is recalling 192 units of VERITAS Collagen Matrix patches because they may have undersized width dimensions. The recall covers US and international distribution.

    Product
    VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0847-2021·2021-01-20

    Visby Medical Recalls 282 COVID-19 Test Kits for Labeling Errors

    Visby Medical is recalling 282 COVID-19 test kits because some boxes incorrectly state the product is CLIA Waived and some components expire before the kit expiration date.

    Product
    visby medical COVID-19 Test kit *** An in vitro diagnostic for the qualitative detection of SARS-CoV-2 - Product Usage: The Visby Medical COVID-19 Test is only for use under the Food and Drug Administration s Emergency Use Authorization.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0844-2021·2021-01-20

    Ortho VITROS Chemistry TP Slides Recalled for Eltrombopag Interference

    Ortho Clinical Diagnostics is recalling VITROS Chemistry TP Slides because the drug eltrombopag can interfere with total protein measurements.

    Product
    VITROS Chemistry Products TP Slides- IVD measure total protein (TP) concentration in serum and plasma using VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems Product Code: 8392292
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0860-2021·2021-01-20

    Medtronic Intellis Spinal Cord Stimulator Software Recall

    Medtronic is recalling the Intellis Spinal Cord Stimulator software due to a defect that prevents clinicians from programming the implantable neurostimulation device.

    Product
    Medtronic Intellis Spinal Cord Stimulator, Model Number A710, Clinical Programmer application version 1.3.80 - Product Usage: intended for use by clinicians in the programming of the following Medtronic neurostimulators (external and implantable) for pain therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0845-2021·2021-01-20

    Ortho Clinical Diagnostics Recalls VITROS XT Chemistry Products ALB-TP Slides

    Ortho Clinical Diagnostics is recalling VITROS XT Chemistry Products ALB-TP Slides due to potential interference from the drug eltrombopag.

    Product
    VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) - IVD quantitatively measures total protein (TP) concentration in serum and plasma using VITROS XT 3400 Chemistry Systems and VITROS XT 7600 Integrated Systems Product Code: 6844293
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0224-2021·2021-01-20

    KVK-Tech Recalls Benzhydrocodone and Acetaminophen Tablets Due to Impurity

    KVK-Tech, Inc. is recalling 528 bottles of Benzhydrocodone and Acetaminophen Tablets because the N-Oxide impurity exceeded specifications during stability testing.

    Product
    Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, Manufactured for: KVK-Tech, Inc., Newtown, PA 18940 USA, NDC 10702-344-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0223-2021·2021-01-20

    US Compounding Recalls Succinylcholine Chloride Injection Due to Labeling Error

    US Compounding Inc is recalling 1,534 syringes of Succinylcholine Chloride Injection because the lot number and expiration date were printed in the wrong position, making them illegible.

    Product
    Succinylcholine Chloride PF Inj. 200 mg/10 mL, 10 mL single use syringes, Rx only, US Compounding, 1270 Don's Lane, Conway, AR 72032
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·21070·2021-01-19

    Rapala Recalls Rechargeable Fillet Knives Due to Fire Hazard

    Rapala USA is recalling about 128,000 rechargeable fillet knives because the batteries can overheat and catch fire if non-Rapala chargers are used.

    Product
    Rapala® Rechargeable Fillet Knives (Item No. RRFN)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E004000·2021-01-19

    Auxbeam Headlight Bulb Recall for Excessive Glare and Brightness

    Guangzhou Zhilan E-Commerce is recalling specific Auxbeam headlight bulbs sold on Amazon that may create excessive glare for oncoming drivers, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2021·2021-01-15

    Nestlé Prepared Foods recalls pepperoni hot pockets due to possible foreign matter contamination

    The USDA Food Safety and Inspection Service is recalling approximately 762,615 pounds of not-ready-to-eat pepperoni hot pockets because they may contain glass and hard plastic fragments. One consumer reported a minor oral injury, but no additional illness cases were reported.

    Product
    Nestlé Prepared Foods Recalls Not-Ready-to-Eat Pepperoni Hot Pockets Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V011000·2021-01-15

    Ford Escape rear drive axle lubricant defect may cause loss of control

    Ford is recalling approximately 147 2020 Ford Escape vehicles and related models due to inadequate lubricant in the rear drive unit, which may cause the rear axle to seize and result in loss of vehicle control and crash risk.

    Product
    FORD — FORD, LINCOLN ESCAPE, CORSAIR, EDGE, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V013000·2021-01-15

    2021 KZRV Recreational Trailers Recalled for Improper Microwave Circuit Protection

    KZRV recalls 2021 Escape, Sonic, and Sportsmen Classic trailers with microwave circuits on improper 20-amp circuit breakers (should be 15-amp), creating fire risk. Owners should request free replacement from KZRV.

    Product
    KZRV — KZRV ESCAPE, SONIC, SPORTSMEN CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V010000·2021-01-14

    2019-2021 Honda Odyssey fuel tank assembly recall due to fire risk

    Braun Corporation is recalling certain 2018-2021 Honda Odyssey vehicles due to a fuel tank assembly defect that may cause fuel leaks, creating a potential fire risk. No injuries have been reported.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21719·2021-01-14

    Scalpa Numb Topical Anesthetic Cream Recalled for Child-Resistant Packaging Failure

    Scalpa Inc. is recalling Scalpa Numb Maximum Strength Topical Anesthetic Cream because the packaging does not meet child-resistant requirements, posing a poisoning risk to young children.

    Product
    Scalpa Numb Maximum Strength Topical Anesthetic Cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide