State

Missouri product recalls

20,371 recalls have nationwide distribution and so reach Missouri. 0 additional recalls listed Missouri specifically in their distribution scope.

About recalls in Missouri

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Missouri consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

16201–16225 of 20371

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 (Drugs)·D-1256-2022·2022-07-27
HYDROmorphone HCl Injection Syringes Recalled for Sterility Assurance
Nephron Sterile Compounding Center is recalling HYDROmorphone HCl Injection syringes nationwide due to lack of assurance of sterility. The recall affects 12,900 syringes across two manufacturing lots.
Product
HYDROmorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL) syringes, 5 x 30 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: 69374-529-30
Category
Drug
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 (Drugs)·D-1280-2022·2022-07-27
Anticoagulant Sodium Citrate Solution Recalled for Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling 85,300 pre-filled syringes of Anticoagulant Sodium Citrate Solution due to failure to assure sterility. Affected patients should contact their healthcare provider.
Product
Anticoagulant Sodium Citrate Solution, USP 4%, 200 mg/5 mL (40 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: 69374-906-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1258-2022·2022-07-27
FDA Recalls HYDROmorphone Injection Syringes Due to Sterility Concerns
Nephron Sterile Compounding Center is recalling 3,740 HYDROmorphone injection syringes due to lack of assurance of sterility. The affected lot was distributed nationwide.
Product
HYDROmorphone HCl Injection, USP, 50 mg/50 mL (1 mg/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. Extension, West Columbia, SC 29172, NDC: 69374-559-50
Category
Drug
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 (Devices)·Z-1446-2022·2022-07-27
Cervical spinal implant connectors may have insufficient clamping force
Aesculap S4 Cervical Cross Connectors used in spinal fusion surgery may have insufficient clamping force, potentially causing movement of the connectors on the rods or wear debris.
Product
AESCULAP S4 Cervical Cross Connector L 28-33mm, S4C CROSS CONNECTOR VARIABLE 28-33MM, SW115T. Used in spinal fusion 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 (Food)·F-1488-2022·2022-07-27
Honeymoons Milk Chocolate Pecan recalled for undeclared tree nuts
Queen Bee Gardens is recalling Honeymoons Milk Chocolate Pecan candies due to the potential presence of undeclared tree nuts. Consumers with tree nut allergies should not consume this product.
Product
Honeymoons Milk Chocolate Pecan. PLU Code: 788394 14684 8. Ingredients: Honey, milk chocolate (sugar, milk, cocoa butter, chocolate liquor, sunflower lecithin and pure vanilla), pecans, butter (pasteurized cream, salt) cream, nonfat dry milk, whey, sunflower lecithin, algin, a
Category
Food
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 (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-1403-2022·2022-07-27
Radiation treatment planning software fails to propagate treatment course data
RayStation 9B SP1 radiation treatment planning software has an issue where treatment course information may not be propagated to other systems in some workflows. This could potentially affect treatment planning accuracy.
Product
RayStation 9B SP1. For radiation treatment planning.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1496-2022·2022-07-27
Truffle Dark Gift Box Recalled for Undeclared Tree Nuts
Queen Bee Gardens recalls Truffle Dark Gift Box due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a risk to consumers with tree nut allergies.
Product
Truffle Dark Gift Box, 12 pc., 6 oz. PLU Code: 788394 17660 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1269-2022·2022-07-27
FDA Recalls Nephron Cardioplegia Solution Over Sterility Assurance Concerns
Nephron Sterile Compounding Center is recalling del Nido Cardioplegia Solution due to lack of assurance of sterility. The 1765 bags affected were distributed nationwide.
Product
del Nido Cardioplegia Solution 1000 mL (1000 mL) Single-Dose Container IV bag, 4 x 1 IV Bag per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-984-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1275-2022·2022-07-27
Phenylephrine HCl injection recalled for lack of sterility assurance
Nephron Sterile Compounding Center recalls Phenylephrine HCl Injection syringes nationwide due to lack of sterility assurance. Patients with affected lots should contact their healthcare provider.
Product
Phenylephrine HCl Injection, USP, 0.8 mg/10 mL (80 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: 69374-956-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1424-2022·2022-07-27
Randox Cholesterol In Vitro Diagnostic Kits Fail Stated Performance Specifications
Randox Cholesterol diagnostic kits fail to meet stated performance specifications. Calibration issues cause quality control results to fall outside acceptable ranges, potentially delaying test results.
Product
Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1264-2022·2022-07-27
Lidocaine HCl injection syringes recalled due to sterility assurance failure
Nephron Sterile Compounding Center has recalled 37,310 syringes of Lidocaine HCl Injection USP 1% nationwide due to lack of assurance of sterility. Affected lots expire between August and October 2022.
Product
Lidocaine HCl Injection, USP 1%, 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: 69374-985-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1461-2022·2022-07-27
Queen Bee Gardens Huckleberry Truffles Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Huckleberry Truffles because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide via internet.
Product
Huckleberry Truffle. Net wt. 1.4 oz. PLU Code: 788394 11057 3. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], HONEY, "Ivory" chocolate (sugar, cocoa butter, whole & non-fat milk solids, sunflower lecith
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1487-2022·2022-07-27
Chocolate Cashew Candy Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honeymoons Ivory Chocolate Cashew candy because it may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts, which can cause severe allergic reactions.
Product
Honeymoons Ivory Chocolate Cashew. PLU Code: 788394 14900 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1255-2022·2022-07-27
HYDROmorphone Injection Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center recalled 22,805 pre-filled syringes of HYDROmorphone HCl Injection due to lack of sterility assurance. Six lot numbers were distributed nationwide.
Product
HYDROmorphone HCl Injection, USP, 10 mg/50 mL (0.2 mg/mL) syringes, 5 x 50 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: 69374-529-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1464-2022·2022-07-27
Bee Energy Bar recalled due to undeclared tree nuts
Queen Bee Gardens is recalling Bee Energy Bars due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Consumers with tree nut allergies should not consume this product.
Product
Bee Energy Bar. Net wt. 1.5 oz. PLU Code: 788394 18559 5. Ingredients: Dark chocolate (sugar, chocolate liquor, cocoa butter, milk fat [butter], sunflower lecithin, pure vanilla), honey, almonds, butter (pasteurized cream, salt), coconut, gluten free oats, dried cranberries
Category
Food
Distribution
Distributed nationwide
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 (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 (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 (Devices)·Z-1448-2022·2022-07-27
Cervical spinal implant connectors may fail to maintain proper clamping force
Aesculap Implant Systems has recalled certain cervical spine implant connectors due to insufficient clamping force. The defect may allow movement on the rods or cause microparticle abrasion.
Product
AESCULAP S4 Cervical Cross Connector L 42-58mm, S4C CROSS CONNECTOR VARIABLE 42-58MM, product code SW117T. Used in spinal fusion surgery.
Category
Medical Device
Distribution
Distributed nationwide