State

Idaho product recalls

73,478 recalls have nationwide distribution and so reach Idaho. 3,523 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total: 3,523
Critical: 364
Severe: 1,217
Most recent: 2026-10-14

Of the 3,523 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,217 (35%) are Severe.

Which agencies issued them

These figures cover only the 3,523 recalls whose distribution notice names Idaho specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20626–20650 of 77001

HighFDA (Drugs)·D-1249-2022·2022-07-27
Compounded Injectable Medications Recalled for Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling 2,315 pre-filled syringes due to lack of sterility assurance. The compounded injectable medication was distributed nationwide.
Product
Bupivacaine HCl 150 mg (3.0 mg/mL), Ketorolac Tromethamine 60 mg (1.2 mg/mL), Ketamine HCl 60 mg (1.2 mg/mL) Injection, 50 mL syringes, 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 12th St.…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1468-2022·2022-07-27
QBee Sea Salt Caramel Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling QBee Sea Salt Caramel due to undeclared tree nuts. The affected product was sold at ten retail locations in Colorado, New Mexico, and Wyoming, and via internet sales.
Product
QBee Sea Salt Caramel. Net wt. 1 oz. PLU Code: 788394 11010 8.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1434-2022·2022-07-27
BD Connecta Stopcock recalled for potential housing leakage risk
Becton Dickinson is recalling BD Connecta Stopcocks due to potential leakage at the housing component. The defect may interrupt treatment and expose patients to biohazardous material.
Product
BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1279-2022·2022-07-27
Sodium Bicarbonate Injection USP recalled for lack of sterility assurance
Nephron Sterile Compounding Center recalls 36,354 pre-filled syringes of Sodium Bicarbonate Injection due to lack of sterility assurance. The medication was distributed nationwide.
Product
8.4% Sodium Bicarbonate Injection, USP, 4.2 g/50 mL (84 mg/mL) 1 mEq/mL syringe, packaged in 1 x 50 mL Pre-Filled Syringe per carton, 30 x 1 syringe carton per case, Rx Only Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-214-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1411-2022·2022-07-27
Medical Device Recall: Hill-Rom PRO+ Mattress Microclimate Feature Failure
Hill-Rom PRO+ mattresses are being recalled for a Microclimate Management feature failure that could increase pressure ulcer risk in patients. The recall affects 200 units distributed in the US and Canada.
Product
Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1444-2022·2022-07-27
Aesculap S4 Cervical Cross Connector Spinal Implant System Recalled for Clamping Failure
Aesculap Implant Systems is recalling the AESCULAP S4 Cervical Cross Connector (product code SWT113T) used in spinal fusion surgery. The connectors may not clamp properly onto rods, potentially causing movement and wear particles.
Product
AESCULAP S4 Cervical Cross Connector L24mm, S4C CROSS CONNECTOR FIXED 24MM, product code SWT113T. Used in spinal fusion surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1429-2022·2022-07-27
Spinal fixation removal key fracture risk under misuse conditions
The ENNOVATE MIS removal key used in spinal fixation systems may fracture if the 90-degree angle is not maintained during use. A product redesign is underway.
Product
ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1402-2022·2022-07-27
Stryker Triton Canister Scanning Labels Recalled Due to Color Variance
Stryker is recalling Triton Canister Scanning Labels that may have color variance issues, potentially resulting in lower-than-expected blood loss estimates. The recall affects 16,700 units distributed nationwide.
Product
Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label (component part number 11032). A software application used to help estimation of blood loss. Used with blood bearing canisters and accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1281-2022·2022-07-27
Succinylcholine Chloride Injection Recalled for Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling 18,840 syringes of Succinylcholine Chloride Injection nationwide because the manufacturing process cannot be assured to have maintained sterility.
Product
Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/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: 69374-919-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1436-2022·2022-07-27
BD Connecta 3-Way Stopcocks Recalled Due to Potential Leakage
Becton Dickinson recalls BD Connecta 3-Way Stopcocks due to potential leakage at the housing that may delay treatment and expose patients to biohazardous material.
Product
BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1532-2022·2022-07-27
Lemon Muffins Recalled Due to Plastic Material Contamination
Portland Specialty Baking is recalling Lemon Muffins due to plastic material contamination. The affected product was distributed in California, Idaho, and Oregon.
Product
Lemon Muffins, item # 802387, are packaged in paper tray and covered with plastic film shrink wrap. Each tray contains 6 pieces and there are 6 trays per master case. PSB (Portland Specialty Baking) master case label is read in parts: "***PSB***LEMON MUFFINS *** 802387***6/36…
Category
Food
Distribution
3 states
HighFDA (Drugs)·D-1267-2022·2022-07-27
Morphine Sulfate Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Morphine Sulfate Injection syringes distributed nationwide due to lack of assurance of sterility. Approximately 43,385 syringes are affected.
Product
Morphine Sulfate Injection, USP, 2 mg/2 mL (1 mg/mL) syringe, packaged in 5 x 2 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: 69374-979-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1454-2022·2022-07-27
Carmel Classic Truffle Recalled for Undeclared Tree Nuts
Queen Bee Gardens recalled Carmel Classic Truffle candies because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts). Consumers with tree nut allergies should not consume this product.
Product
Carmel Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 110005 4. Ingredients: Milk chocolate, honey, ivory chocolate, butter (pasteurized cream & salt), cream, non-fat dry milk, caramel flavor, whey, agar, algin & lecithin.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1495-2022·2022-07-27
Truffle Gift Box Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Truffle Gift Boxes due to undeclared tree nuts that may pose a hazard to allergic consumers. Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Truffle Gift Box PLU Code: 788394 17655 5
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1252-2022·2022-07-27
Fentanyl Citrate Injection Recall Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Fentanyl Citrate Injection nationwide due to lack of assurance of sterility. Approximately 9,410 bags distributed to healthcare facilities are affected.
Product
Fentanyl Citrate in 0.9% Sodium Chloride Injection, USP, 2500 mcg/250 mL (10 mcg/mL*) bags, packaged as 10 x 1 IV bag per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-523-21
Category
Drug
Distribution
Distributed nationwide
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-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 (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