State

Delaware product recalls

73,388 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: 2026-09-23

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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21901–21925 of 76826

SevereFDA (Drugs)·D-0856-2022·2022-05-18
SyrSpend SF Suspending Base Recalled for Burkholderia Contamination
Fagron is recalling SyrSpend SF Suspending Base, Cherry Flavored (NDC 51552-1123-5 and 51552-1123-9) due to contamination with Burkholderia gladioli. This FDA Class I recall affects medication used in compounding.
Product
SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only, Manufactured for Fagron, Inc., St. Paul, MN 55120.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1009-2022·2022-05-18
FDA Recalls Accula SARS-CoV-2 Test for False Positive Risk
Mesa Biotech is recalling approximately 6,162 units of the Accula SARS-CoV-2 Test due to an increased risk of false positive results, which could delay correct diagnosis and treatment.
Product
Accula SARS-CoV-2 Test, REF: COV4100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1057-2022·2022-05-18
Chemotherapy Infusion Bag Adaptor May Disconnect and Spill Hazardous Drugs
Simplivia Healthcare is recalling OnGuard2 CSTD Bag Adaptors because they may disconnect from infusion bags, potentially spilling hazardous medications.
Product
OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1043-2022·2022-05-18
Medtronic IN.PACT AV Balloon Catheter: Damaged Packaging May Affect Sterility
Medtronic is recalling IN.PACT AV paclitaxel-coated balloon catheters because packaging damage may result in loss of sterility. The devices were distributed worldwide and in the United States.
Product
Medtronic IN.PACT AV, Paclitaxel-coated PTA Balloon Catheter, REF: IAV06008008P, Sterile EO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V352000·2022-05-18
Can-Am Recalls 2015-2019 Spyder RT and F3 for Sprocket Defect
Bombardier is recalling 2015-2019 Can-Am Spyder RT and F3 motorcycles because a defective front sprocket may wear prematurely, causing a loss of drive power and increasing crash risk.
Product
CAN-AM — CAN-AM SPYDER RT, SPYDER F3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1050-2022·2022-05-18
O-Organic Sea Salt Popcorn Recalled for Potential Milk Allergen Contamination
Snak King Corporation recalls O-Organic Sea Salt Popcorn due to milk allergen found in the production line's recycle chute. Consumers with milk allergies should not consume this product.
Product
12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-1055-2022·2022-05-18
Flexible Bronchoscope Recalled Due to Inadequate Disinfection Process
Karl Storz is recalling flexible bronchoscopes due to potential failure of the disinfection process. The devices may not eliminate microorganisms adequately, posing an infection risk to patients.
Product
11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V351000·2022-05-18
2022 Lucid Air Display Wiring Harness May Disable Critical Safety Screens
Lucid is recalling 2022 Air vehicles because the display wiring harness may not be secured properly, potentially disabling screens that show speedometer, gear selection, and warning lights.
Product
LUCID — LUCID AIR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0855-2022·2022-05-18
MVASI Cancer Drug Recalled for Loose Container Crimp
Amgen is recalling specific lots of MVASI (bevacizumab-awwb) injection due to a loose crimp defect in the container that could compromise container integrity. Patients should contact their healthcare provider.
Product
MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by Amgen Inc. Thousand Oaks, CA 91320-1799, NDC 55513-0206-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1074-2022·2022-05-18
Phototherapy Units Recalled for Software Bug Causing Incorrect Dosing
Daavlin's 4 Series CX phototherapy units are recalled due to a software defect that can cause incorrect dosing (over or under) when resuming interrupted treatments.
Product
4 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. M4 Ser CX 311-20 120-240V 50/60Hz, item # 807QS0020CX6.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1055-2022·2022-05-18
Bwell Bird's Nest Lychee Beverage recalled for deficient packaging and spoilage risk
Eastland Food Corporation is recalling Bwell Bird's Nest Beverage in Lychee Flavor due to deficient packaging material that could lead to premature spoilage. Approximately 1,699 cases were distributed to retail stores across 33 states.
Product
Bwell Bird's Nest Beverage Lychee Flavor NET 8.45 FL OZ (250mL) UPC 8373726350 24 bottles per case
Category
Food
Distribution
34 states
HighFDA (Devices)·Z-1072-2022·2022-05-18
Radial Head Replacement System implant: contraindications added to safety instructions
Synthes has updated safety instructions for its Radial Head Replacement System implant with absolute contraindications for use in patients with infection, sepsis, or osteomyelitis. The FDA has classified this as a Class II recall.
Product
Radial Head Replacement System Implant is a one-piece, stemmed radial head replacement. The radial head is available in diameters of 19, 22 and 25mm. The radial stems range from 5.5 to 8.5mm in diameter and from 21 24mm in length.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1071-2022·2022-05-18
TMJ Arthroscopy Drape incorrectly labeled latex-free when containing latex
Microtek Medical Inc. is recalling TMJ Arthroscopy Drapes that contain latex but were mislabeled as latex-free, posing an allergic reaction risk to patients and healthcare workers with latex sensitivities.
Product
TMJ Arthroscopy Drape, 85''x 96''
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1036-2022·2022-05-18
Spine Surgery Instrument Sets Recalled for Sterilization Defect
American Contract Systems is recalling ACS Spine Pack and ACS Lumbar/Back Set Up Tray surgical instrument sets due to improper sterilization with excess ethylene oxide. The affected sets were distributed in Illinois, Missouri, Nebraska, and Texas.
Product
1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1070-2022·2022-05-18
Flexible video uretero-renoscopes recalled for inadequate sterilization
Karl Storz Endoscopy is recalling Flexible Video-Uretero-Renoscope (FLEX-XC) models because they may fail to achieve adequate disinfection, creating potential microbial contamination risk.
Product
11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSE 11278VSEK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSU 11278VSUK Flexible Video-Uretero-Renoscope (FLEX-XC) Z18447US-BC (03/2018); 11278VSUA 11278VSUAK…
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-1063-2022·2022-05-18
Karl Storz HD Cysto-Urethroscope recalled for disinfection failure
Karl Storz is recalling HD-VIEW Flexible HD Cysto-Urethroscope models that fail to adequately disinfect during processing, creating a potential infection risk. All units manufactured since January 2018 are affected.
Product
11272VH-TL 11272VHK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC (10-2021) 11272VHU-TL 11272VHUK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC (10-2021)
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-1054-2022·2022-05-18
KARL STORZ Nasopharyngolaryngoscope Disinfection Failure Affects 14 States
The FDA is recalling KARL STORZ Slim Nasopharyngolaryngoscope models 11001RD1 and 11001RDK1 because they fail to achieve adequate disinfection, potentially allowing microorganisms to persist on the device and transmit between patients.
Product
11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1066-2022·2022-05-18
Flexible Cystoscopes Recalled for Inadequate Disinfection Process
Karl Storz Flexible Cystoscope units may not be properly disinfected because the disinfection process fails to achieve the expected reduction of microorganisms. All units manufactured since January 2018 are potentially affected.
Product
11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (08-2018)
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-1038-2022·2022-05-18
ACS IR Angio Pack Sterilization Process Defect Recall
The ACS IR Angio Pack from American Contract Systems, Inc. was sterilized using ethylene oxide at higher than specification concentration. No illnesses or injuries have been reported.
Product
ACS IR - Angio Pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0860-2022·2022-05-18
Esomeprazole magnesium delayed-release capsules recalled for impurity specification failure
Mylan Institutional Inc. is recalling Esomeprazole Magnesium Delayed-Release Capsules 20 mg due to failed impurity specifications detected during stability testing. 555 cartons of affected lots were distributed nationwide.
Product
Esomeprazole Magnesium Delayed-Release Capsules, USP 20 mg, packaged in Unit Dose Blister Cards of 6 (10 cards of 6 Capsules each per carton), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC 42292-009-16
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1073-2022·2022-05-18
Daavlin 1 Series CX Phototherapy Units Recalled for Software Dosing Error
Daavlin is recalling 1 Series CX phototherapy units due to a software bug that swaps calibration distance settings when resuming interrupted treatments, resulting in incorrect dosing.
Product
1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. Models: [1 Ser CX 305-4 120-240V 50/60Hz, item # 06OS0004CX6], [1 Ser CX 311-4 120-240V 50/60Hz CE, item # 807OS0004CX5], [1 Ser CX 311-4 120-240V 50/60Hz, item…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1075-2022·2022-05-18
X-ray Imaging Systems Have Reversed Spine Positioning Labels
Shanghai United Imaging's digital X-ray systems may display reversed spine positioning labels, potentially causing misdiagnosis and unnecessary repeat radiation exposure for patients.
Product
Digital Medical X-ray Imaging System, Model: uDR 596i, uDR 592h
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1064-2022·2022-05-18
Karl Storz Flexible Video Urethro Cystoscope Recalled for Inadequate Disinfection
Karl Storz is recalling multiple Flexible Video Urethro Cystoscope models because they may fail to achieve proper disinfection between procedures, posing a risk of microbial contamination.
Product
11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018); 11272VNU 11272VNUK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-1065-2022·2022-05-18
Cysto-Urethroscope Disinfection Process Failure Affects Serial Numbers Since 2018
Karl Storz Endoscopy is recalling Flexible Video Cysto-Urethroscopes due to a disinfection process failure that may not adequately eliminate microorganisms. Affected units have been distributed nationwide and internationally since January 2018.
Product
11272VUE 11272VUEK Flexible Video Cysto-Urethroscope 96136031USCA V1.1 (04/2021); 11272VUE-R 11272VUEK-R Flexible Video Cysto-Urethroscope 96136031USCA V1.1 (04/2021)
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-1047-2022·2022-05-18
Bronchovideoscope Reprocessing Instructions Updated Due to Sterilization Concerns
Olympus is issuing updated instructions for reprocessing its EVIS EXERA bronchovideoscopes to ensure proper sterilization and disinfection procedures. Improper reprocessing could compromise device safety.
Product
BF-3C160: EVIS EXERA Bronchovideoscope
Category
Medical Device
Distribution
Distributed nationwide