State

Delaware product recalls

73,366 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 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19526–19550 of 76804

HighFDA (Food)·F-0054-2023·2022-10-26
Lyons Ready Care Thickened Apple Honey Nectar Recalled Due to Spoilage
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Honey Nectar due to indications of product spoilage. The nationwide recall affects 645 cases with specific lot numbers and best-by dates in March 2023.
Product
Lyons Ready Care Thickened Apple Honey Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighFDA (Devices)·Z-0100-2023·2022-10-26
Synthes SPEED implant recall: drill guide size mismatch in surgical kit
Synthes is recalling SPEED 9X10X10mm surgical implant kits nationwide due to an incorrect-size drill guide that will not properly prepare bone for the implant, creating potential for bone damage.
Product
SPEED 9X10X10mm Continuous Compression Implant, Product No. SE-0910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0112-2023·2022-10-26
Medicina Reusable Oral Syringe Recalled for Unapproved Plunger Material
Medicina Uk Ltd is recalling Medicina Reusable Oral syringes because the plunger was manufactured with polyethylene instead of the required polypropylene material. The 11,100 affected syringes do not meet raw material specifications.
Product
Medicina Reusable Oral syringe 1ml Code: OTH01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0113-2023·2022-10-26
Reusable Oral Syringe Recalled for Unapproved Plunger Material
Medicina UK Ltd is recalling Reusable Oral Syringes because plungers were manufactured from unapproved polyethylene instead of the specified polypropylene material.
Product
Medicina Reusable Oral syringe 5ml Code: OTH05
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0068-2023·2022-10-26
Tastykake Glazed Caramel Apple Pie Recalled for Undeclared Soy
Flowers Foods is recalling Tastykake Glazed Caramel Apple Pie because some packages contain undeclared soy lecithin, a major food allergen. Consumers with soy allergies should not consume this product.
Product
TASTYKAKE GLAZED CARAMEL APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 08618 6 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0102-2023·2022-10-26
ARROW Midline Catheter Kit Mislabeled with Wrong Device Type
ARROW INTERNATIONAL Inc. is recalling an ARROW Pressure Injectable Arrowgard Blue Advance Midline Catheter Kit due to mislabeling. The package labels incorrectly specify a double-lumen 5.5 French catheter, but the kit contains a single-lumen 4.5 French catheter.
Product
ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF ASK-41552-JHVA1. For peripheral access to the venous system for intravenous therapy, blood sampling, infusion, and pressure injection of contrast media.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0060-2023·2022-10-26
Lyons Magnus Thickened Cranberry Cocktail Nectar Recalled for Product Spoilage
Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Nectar due to indication of product spoilage. Approximately 2094 cases were distributed nationwide.
Product
Imperial Thickened Cranberry Cocktail Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighFDA (Devices)·Z-0092-2023·2022-10-26
IV extension set recall for potential joint failure and leakage risk
B. Braun is recalling CARESITE SMALLBORE EXT SET T-PORT 5 IN. devices due to potential bonded joint failure that could cause leakage or detachment during use. The malfunction may result in delayed therapy, bloodstream infection risk, and exposure to hazardous medications.
Product
CARESITE SMALLBORE EXT SET T-PORT 5 IN., Product Code 470114, 100 units per carton. The A6 Access Device is a valve intended for the aspiration, injection or gravity/pump flow of IV fluids and blood.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0043-2023·2022-10-26
Market Pantry White Fudge Animal Cookies Recalled for Metal Contamination
Market Pantry White Fudge Animal Cookies sold at Target may contain metal fragments. D. F. Stauffer Biscuit Co is recalling 883 cases distributed nationwide.
Product
White frosted animal cookies with multi-colored non-pareils in a 44oz plastic jug labeled "Market Pantry White Fudge Animal Cookies"
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0048-2023·2022-10-26
Seeking Health Optimal Multivitamin Chewable Supplement Recalled for Excess Copper
Seeking Health LLC is recalling Optimal Multivitamin Chewable Dietary Supplement tablets because lab testing found higher copper levels than stated on the label.
Product
Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product is packaged in white non-flex plastic bottles. UPC: 810007520902. Product labels read in part: Adults and children age 4 and over; Chew 2 tablets daily.…
Category
Consumer Product
Distribution
51 states
HighFDA (Food)·F-0061-2023·2022-10-26
Imperial Thickened Cranberry Cocktail Honey Recalled for Product Spoilage
Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Honey due to indication of product spoilage. Consumers who have purchased affected cases should stop using the product.
Product
Imperial Thickened Cranberry Cocktail Honey packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighNHTSA·22V804000·2022-10-26
Rearview camera display malfunction in 2022 Lamborghini Urus vehicles
The infotainment system in certain 2022 Lamborghini Urus vehicles may become damaged, causing the rearview camera display to become inoperative. This reduces rear visibility and increases the risk of a crash.
Product
LAMBORGHINI — LAMBORGHINI URUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0066-2023·2022-10-26
Mrs. Freshley's Cherry Fruit Pie recalled for undeclared soy lecithin
Flowers Foods is recalling Mrs. Freshley's Cherry Fruit Pie due to undeclared soy lecithin. Soy is a major allergen; consumers with soy allergies should not consume the product.
Product
Mrs. Freshley's Cherry Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 0081 0 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP, LLC, 5987 SOUTH ROYAL ATLANTA DR, TUCKER, GA 30084
Category
Food
Distribution
50 states
HighNHTSA·22V806000·2022-10-26
Multiple 2021-2022 Audi models recalled for rearview camera failure
Volkswagen Group of America is recalling certain 2021-2022 Audi vehicles. The infotainment system may fail to display the rearview camera, reducing rear visibility and increasing crash risk.
Product
AUDI — AUDI A3, Q8, Q3, Q7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0013-2023·2022-10-26
Acyclovir Sodium Injectable Recalled for Particulate Matter
AuroMedics Pharma is recalling Acyclovir Sodium injection due to dark red, brown, and black particulate matter found in vials. Approximately 89,400 vials were distributed nationwide.
Product
ACYCLOVIR SODIUM — ACYCLOVIR SODIUM (ACYCLOVIR SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0062-2023·2022-10-26
Lyons Ready Care Thickened Apple Juice Recalled for Spoilage Indication
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Juice due to indication of product spoilage. The recall affects 320 cases distributed nationwide.
Product
Lyons Ready Care Thickened Apple Juice packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighFDA (Devices)·Z-0110-2023·2022-10-26
Oral Tip Syringes Recalled Due to Unapproved Plunger Material
Medicina Oral Tip Syringes are being recalled because the plunger component was made with polyethylene instead of the approved polypropylene material. No illnesses or injuries have been reported.
Product
Medicina Oral Tip Syringe 1ml Code: OT01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0090-2023·2022-10-26
ULTRASITE US04TL Extension Sets recalled for bonded joint failure risk
B. Braun is recalling ULTRASITE Extension Sets because the bonded joint has a high probability of failure during use. Device failure could cause leakage, bloodstream infections, and delays in therapy.
Product
ULTRASITE US04TL Smallbore T-Port Extension Set, Product Code 474515, 100 units per carton. to provide needle-free access on I.V. and Extension Sets
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0104-2023·2022-10-26
Lithium diagnostic assay may display falsely elevated results on Atellica CH analyzer
The Atellica CH Lithium_2 diagnostic assay may produce falsely elevated lithium readings on the Atellica CH 930 analyzer, potentially leading to incorrect medication dosage adjustments. No illnesses have been reported.
Product
Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11532401. in vitro diagnostic assay
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0109-2023·2022-10-26
Medicina Oral Tip Syringe Recall Due to Unapproved Plunger Material
Medicina Uk Ltd is recalling 12,000 Oral Tip Syringes (Code: OT005) because the plunger component was manufactured with polyethylene instead of the approved polypropylene material. The syringes do not meet raw material specifications.
Product
Medicina Oral Tip Syringe 0.5ml Code: OT005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0105-2023·2022-10-26
Medical device assay may report falsely elevated lithium levels
Siemens' Atellica CH Lithium diagnostic assay may falsely report elevated lithium levels, potentially leading to incorrect dose adjustments in patients on lithium therapy.
Product
Atellica CH Lithium (Li), Siemens Material Number 11097535. in vitro diagnostic assay
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0011-2023·2022-10-26
Rifampin Capsules recalled due to excessive impurity levels
Golden State Medical Supply Inc. is recalling Rifampin Capsules, USP, 300 mg, because samples exceeded acceptable limits for 1-Methyl-4-Nitrosopoperazine (MNP), an impurity. Multiple lot numbers were distributed nationwide.
Product
Rifampin Capsules, USP, 300 mg, packaged in a) 30-count bottle (NDC 51407-323-30), b) 60-count bottle (NDC 51407-323-60), c) 100-count bottle (NDC 51407-323-01), Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V807000·2022-10-26
Volkswagen Atlas and Cross Sport trailing arm bolt defect recall
Volkswagen is recalling certain 2022 Atlas and 2022-2023 Cross Sport vehicles because driver-side rear trailing arm bolts may loosen and fall out, risking loss of vehicle control.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0101-2023·2022-10-26
DePuy Synthes Hammertoe Implants Recalled for Incorrect Drill Guide Size
Synthes (USA) Products LLC is recalling 196 DePuy Synthes Hammertoe Continuous Compression Implants due to an incorrect drill guide size that will not properly prepare bone for the implant, creating potential for bone damage.
Product
DePuy Synthes Hammertoe Continuous Compression Implants, Product No. 46.239.001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0095-2023·2022-10-26
BD Vacutainer Blood Alcohol Testing Tubes Recalled for Analytical Interference
BD Vacutainer blood collection tubes are recalled due to isobutylene contamination that may cause false positive results in blood alcohol testing.
Product
BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.
Category
Medical Device
Distribution
Distributed nationwide