State

Illinois product recalls

73,509 recalls have nationwide distribution and so reach Illinois. 11,650 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,650
Critical: 2,050
Severe: 3,017
Most recent: 2026-10-14

Of the 11,650 recalls naming Illinois we have scored against our rubric, 2,050 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,017 (26%) are Severe.

Which agencies issued them

These figures cover only the 11,650 recalls whose distribution notice names Illinois specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22401–22425 of 85159

HighFDA (Drugs)·D-1250-2022·2022-07-27
Epinephrine Injection Recalled Due to Sterility Assurance Failure
Nephron is recalling epinephrine injection syringes nationwide due to lack of sterility assurance. No illnesses have been reported to date.
Product
EPINEPHrine Injection, USP, 0.1 mg/10 mL (10 mcg/mL) syringes, 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th Street Extension, West Columbia SC 29172, NDC: 69374-544-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1479-2022·2022-07-27
Honey Caramels Pecan Pearl Recalled for Undeclared Tree Nuts
Queen Bee Gardens recalls Honey Caramels Pecan Pearl due to potential undeclared tree nuts including almonds, coconut, macadamia, and walnuts that may pose a risk to consumers with allergies.
Product
Honey Caramels Pecan Pearl. Net wt. 5.87 oz. PLU Code: 788394 12804 2. Ingredients: Honey, butter (pasteurized cream & salt), cream, grade A fancy pecans, nonfat dry milk, whey, pure vanilla, lecithin, algin & agar.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1262-2022·2022-07-27
Labetalol Injection Recalled Nationwide Over Sterility Assurance Defect
Nephron Sterile Compounding Center is recalling 184,370 syringes of Labetalol HCl Injection nationwide due to lack of assurance of sterility. Patients using the affected lots should contact their healthcare provider.
Product
Labetalol HCl Injection, USP, 20 mg/4 mL (5 mg/mL) syringe, packaged in 5 x 4 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-946-04
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1248-2022·2022-07-27
Injectable Lidocaine Syringes Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center has recalled 1,380 prefilled lidocaine syringes nationwide due to inability to confirm product sterility.
Product
0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate), 45 mg/5 mL (9 mg/mL) syringes, packaged in 5 x 5 mL Prefilled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1278-2022·2022-07-27
Compounded Sterile Injectable Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center LLC is recalling 2210 syringes of a three-drug compounded injectable due to lack of assurance of sterility.
Product
Ropivacaine HCl 123 mg (2.46 mg/mL), Clonidine HCl 0.04 mg (0.0008 mg/mL), Ketorolac Tromethamine 15 mg (0.3 mg/mL) Injection, 50 mL syringe, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1438-2022·2022-07-27
BD Connecta White 360 Infusion Connector Recalled for Potential Leakage
Becton Dickinson recalls BD Connecta White 360 infusion connectors for potential leakage at the stopcock housing. The defect may interrupt treatment and expose patients to biohazardous materials.
Product
BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1446-2022·2022-07-27
Chuckanut Bay Lemon Cheesecake Bites Recalled for Undeclared Soy Lecithin
Chuckanut Bay Foods is recalling Lemon Cheesecake Bites because the label declares Sunflower Lecithin when the product actually contains Soy Lecithin. Consumers with soy allergies may unknowingly consume these products and experience allergic reactions.
Product
Item 39432-12, Chuckanut Bay DIPPED CHEESECAKE BITES Lemon. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net Wt. 3.2 oz. UPC 6 03812 39432 1. Item 32032-1, Chuckanut Bay Lemon Cheesecake Bites (Dark Compound) BULK. There are 14 pieces…
Category
Food
Distribution
13 states
HighFDA (Food)·F-1459-2022·2022-07-27
German Chocolate Truffle Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling German Chocolate Truffles because they may contain undeclared tree nuts. The recall affects products sold in Colorado, New Mexico, Wyoming, and through nationwide internet sales.
Product
German Chocolate Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11058 0.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1489-2022·2022-07-27
Dark Chocolate Pecan Recalled for Undeclared Tree Nuts
Queen Bee Gardens recalls Honeymoons Dark Chocolate Pecan for undeclared tree nuts including almonds, coconut, macadamia, and walnuts. The product was distributed through retail locations in CO, NM, and WY, and nationwide via internet sales.
Product
Honeymoons Dark Chocolate Pecan. PLU Code: 788394 14720 3.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1449-2022·2022-07-27
Aesculap Sterile Disposable Fleece Drape Recalled Due to Packaging Seal Integrity Issue
Aesculap recalls 4500 sterile disposable fleece drapes (Product code GA414) due to unvalidated packaging seal integrity, which may compromise sterility assurance. Distribution occurred in 14 U.S. states.
Product
Aesculap Sterile disposable fleece drape, Product code: GA414, individually packaged, 50 pieces per shipping unit, product code SZ380R.
Category
Medical Device
Distribution
14 states
HighFDA (Food)·F-1493-2022·2022-07-27
Toffee Bites Patties Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Toffee Bites Patties Gift Boxes due to undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts) that may pose a risk to people with nut allergies.
Product
Toffee Bites Patties Gift Box. Net wt. 3 oz. PLU Code: 788394 17777 4.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1465-2022·2022-07-27
Bee Joyful Bars Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Bee Joyful Bars due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a health risk to consumers with tree nut allergies.
Product
Bee Joyful Bars. Net wt. 1.5 oz. PLU Code: 788394 18565 6. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], sunflower lecithin & pure vanilla), Honey, Butter (Pasteurized cream & Salt), Cream, Coconut…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1433-2022·2022-07-27
Revie Superfoods Heart Beet Smoothie Mix Recalled for Potential Norovirus
Revive Organics is recalling Revie Superfoods Heart Beet 206g Ready-to-Blend smoothie mix due to potential norovirus contamination in frozen raspberries used in the product. Consumers should not consume affected lots.
Product
Revie Superfoods Heart Beet 206g Ready-to-Blend Cardamom + Beet Smoothie Made in Canada UPC 8 53267 00112 5 Revive Superfoods 1880 Bonhill Road, Mississauga, Ontario, Canada
Category
Food
Distribution
4 states
HighFDA (Food)·F-1472-2022·2022-07-27
Honey Caramels Blue Raspberry Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honey Caramels Blue Raspberry due to undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The product poses a serious risk to consumers with tree nut allergies.
Product
Honey Caramels Blue Raspberry. Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag. PLU Code for 5.87 oz. bag: 788394 12675 8.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1391-2022·2022-07-27
Surgical knee implant instrument key may become nonfunctional during assembly
Aesculap is recalling the ENDURO SPECIAL KEY TIB.LOCK.RING (product code NP462R) used in knee replacement surgery because the key pins may be damaged during assembly, causing the instrument to become nonfunctional.
Product
ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during orthopedic implant surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1417-2022·2022-07-27
Hill-Rom Centrella Pro+ surface mattress microclimate management feature failure
Baxter Healthcare is recalling Hill-Rom Centrella Pro+ surface mattresses due to a potential Microclimate Management feature failure that may increase the risk of pressure ulcer development.
Product
Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1277-2022·2022-07-27
Rocuronium Bromide Pre-Filled Syringes Recalled for Sterility Assurance
Nephron Sterile Compounding Center is recalling Rocuronium Bromide Injection syringes nationwide due to lack of assurance of sterility. Approximately 6,340 syringes from lot RC2003B (expiration August 28, 2022) are affected.
Product
Rocuronium Bromide Injection, 50 mg/5 mL (10 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-924-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1448-2022·2022-07-27
Chuckanut Bay cheesecake bites recalled for undeclared soy lecithin
Chuckanut Bay Foods is recalling Dipped Cheesecake Bites (Berry) due to undeclared soy lecithin. The label incorrectly lists sunflower lecithin, potentially endangering consumers with soy allergies.
Product
Item 39421-12, Chuckanut Bay DIPPED CHEESECAKE BITES Berry. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net wt. 3.2 oz per package. UPC 6 03812 39421 5. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CANE SUGAR…
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-1426-2022·2022-07-27
Sensis Vibe Combo Device Recalled for Software Communication Failure
The Sensis Vibe Combo diagnostic system may experience communication failure during patient procedures, causing vital signs data to be unavailable. The recall affects 13 units distributed across multiple U.S. states.
Product
Sensis Vibe Combo with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology Model: 11007642
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1274-2022·2022-07-27
Phenylephrine HCl Injection Recalled for Lack of Sterility Assurance
Nephron is recalling Phenylephrine HCl Injection syringes due to lack of assurance of sterility. Approximately 75,630 syringes distributed nationwide are affected.
Product
Phenylephrine HCl Injection, USP, 0.4 mg/10 mL (40 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-955-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1460-2022·2022-07-27
Grandma's Fudge Classic Truffle Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Grandma's Fudge Classic Truffle due to undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The product may pose a risk to individuals with tree nut allergies.
Product
Grandma's Fudge Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11062 7. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], sunflower lecithin & pure vanilla) honey, butter (pasteurized cream, salt)…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1463-2022·2022-07-27
Truffle Recall: Undeclared Tree Nuts Present Allergen Risk
Queen Bee Gardens is recalling Midnight Gold Classic Truffles for potentially containing undeclared tree nuts, which pose a risk to allergic consumers. Distribution included Colorado, New Mexico, Wyoming, and nationwide online.
Product
Midnight Gold Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11070 2. Ingredients: Dark chocolate, honey, butter (pasteurized cream, salt), cream, non-fat dry milk, whey, almonds, milk chocolate, natural flavor, salt, soda, agar, algin & lecithin.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1455-2022·2022-07-27
Recall: Cherry Classic Truffle Contains Undeclared Tree Nuts
Queen Bee Gardens recalled Cherry Classic Truffles (1.4 oz) due to undeclared tree nuts: pecans, almonds, coconut, macadamia nuts, and walnuts. Consumers with tree nut allergies should not consume this product.
Product
Cherry Classic Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11015 3. Ingredients: Milk chocolate, honey, butter (pasteurized cream & salt), cream, cherries, pecans, non-fat dry milk, whey, agar, algin, lecithin, citric acid & natural flavor.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1482-2022·2022-07-27
Honey Caramels Recalled for Undeclared Tree Nut Allergens
Queen Bee Gardens recalls Honey Caramels Vanilla products that may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts), which can harm consumers with allergies.
Product
Honey Caramels Vanilla. PLU Code: 788394 12332 0 Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1246-2022·2022-07-27
Atropine Sulfate Injection Recalled Nationwide for Sterility Assurance Failure
Nephron Sterile Compounding Center LLC is recalling Atropine Sulfate Injection pre-filled syringes nationwide due to lack of assurance of sterility affecting approximately 13,340 syringes.
Product
Atropine Sulfate Injection, USP 1.2 mg/3 mL (0.4 mg/mL) syringe, packaged in 5 x 3 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility 4500 12th Street Extension, West Columbia, SC 29172, NDC: 69374-935-03
Category
Drug
Distribution
Distributed nationwide