State

Pennsylvania product recalls

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

About recalls in Pennsylvania

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 Pennsylvania 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.

16251–16275 of 20371

HighFDA (Devices)·Z-1420-2022·2022-07-27
Ambu VivaSight 2 DLT endobronchial tubes recalled for cuff leak risk
Ambu Inc. is recalling the VivaSight 2 DLT endobronchial tube system due to reports of cuff leaks or ruptures that could compromise airway security during intubation procedures.
Product
Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning. Catalog numbers 412351000, 412371000, 412391000, 412411000
Category
Medical Device
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-1260-2022·2022-07-27
Ketamine HCl Injection Syringes Recalled Due to Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling Ketamine HCl Injection pre-filled syringes due to lack of assurance of sterility. The recall affects 30,745 syringes distributed nationwide.
Product
Ketamine HCl Injection, USP 30 mg/3 mL (10 mg/mL*) syringes, 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 St. Extension, West Columbia, SC 29172, NDC: 69374-982-33
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1247-2022·2022-07-27
Bupivacaine Injection Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling 6900 syringes of Bupivacaine HCl Injection nationwide due to lack of sterility assurance. No illnesses or injuries have been reported.
Product
0.125% Bupivacaine HCl Injection, USP, 62.5 mg/50 mL (1.25 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. Ext., West Columbia, SC 29172, NDC: 69374-970-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1439-2022·2022-07-27
BD Connecta Plus3 infusion connector recalled for potential stopcock leakage
Becton Dickinson is recalling BD Connecta Plus3 White Blend infusion connectors (Lot 1127328) due to potential stopcock leakage. The defect may interrupt treatment, expose patients to biohazardous material, or cause under-infusion.
Product
BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1425-2022·2022-07-27
Sensis diagnostic tool software may fail to display vital signs
Siemens' Sensis diagnostic tool may lose communication and fail to display vital signs during initial patient exams or after inactivity. Software updates are required.
Product
Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology Model:10764561
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1497-2022·2022-07-27
Valentine Gift Box Recall Due to Undeclared Tree Nuts
Queen Bee Gardens is recalling Valentine Gift Box products that may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Products were distributed through 10 retail locations in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Valentine Gift Box. Net wt. 7.5 oz. PLU Code: 788394 17700 2.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1474-2022·2022-07-27
Honey Caramels Caramel Apple Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honey Caramels Caramel Apple because the product may contain undeclared tree nuts. The recall affects products sold at ten retail locations and online nationwide.
Product
Honey Caramels Caramel Apple. Net wt. 5.87 oz. PLU Code: 788394 12204 0. Ingredients: Honey, butter (pasteurized cream & salt), cream, almonds, nonfat dry milk, whey, natural flavors, lecithin, algin & agar.
Category
Food
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-1485-2022·2022-07-27
Honeymoons Milk Chocolate Cashew recalled for undeclared tree nuts
Queen Bee Gardens is recalling Honeymoons Milk Chocolate Cashew candy due to undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. Consumers with tree nut allergies face potential serious health risks.
Product
Honeymoons Milk Chocolate Cashew. PLU Code: 788394 14828 6
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1414-2022·2022-07-27
Hill-Rom Hospital Mattress Surfaces Recalled for Pressure Ulcer Risk
Baxter Healthcare is recalling 202 Hill-Rom PRO+ mattress surfaces. The microclimate management feature may malfunction, reducing the product's ability to manage heat and moisture, which increases the risk of patient pressure ulcers.
Product
Hill-Rom PRO+ MRS Surface For Versacare mattress, REF P3255A02.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1415-2022·2022-07-27
Medical Bed Mattress Microclimate Failure Increases Pressure Ulcer Risk
Affected Hill-Rom Centrella Pro+ hospital mattresses can fail to properly manage heat and moisture removal, increasing the risk of pressure ulcer development in patients.
Product
Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1257-2022·2022-07-27
HYDROmorphone Injection Recalled Due to Lack of Sterility Assurance
HYDROmorphone HCl Injection 30 mg/30 mL from Nephron Sterile Compounding Center LLC is being recalled nationwide due to lack of assured sterility. The recall affects 18,570 syringes across three lot numbers.
Product
HYDROmorphone HCl Injection, USP 30 mg/30 mL (1 mg/mL) syringe, 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: 69374-559-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1471-2022·2022-07-27
Honey Caramels Almond Coconut Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honey Caramels Almond Coconut due to potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Consumers allergic to tree nuts should not consume this product.
Product
Honey Caramels Almond Coconut. Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag. PLU Code for 5.87 oz bag: 788394 12004 6. Ingredients: Honey, butter (pasteurized cream & salt), cream, almonds, coconut, nonfat dry milk, whey, natural flavors, lecithin, algi
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1486-2022·2022-07-27
Honeymoons Dark Chocolate Cashew Recalled for Undeclared Tree Nuts
Honeymoons Dark Chocolate Cashew products may contain undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product is being recalled from Queen Bee retail locations in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Honeymoons Dark Chocolate Cashew. PLU Code: 788394 14864 4.
Category
Food
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 (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 (Drugs)·D-1285-2022·2022-07-27
Aripiprazole 20mg Tablets Recalled for Failed Dissolution
Apotex Corp. is recalling 2,010 bottles of Aripiprazole Tablets 20mg nationwide due to failed dissolution specifications. Tablets may not dissolve properly, potentially affecting medication effectiveness.
Product
Aripiprazole Tablets, USP 20 mg, packaged in a) 1,000-count bottle (NDC 60505-2676-8, UPC 3 60505 26768 2), b) 30-count bottle (NDC 60505-2676-3, UPC 3 60505 26763 7), Rx only, Manufactured by: Apotex, Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, F
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1265-2022·2022-07-27
Morphine Sulfate Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Morphine Sulfate Injection due to lack of assurance of sterility. The recall affects 5,495 pre-filled syringes distributed nationwide.
Product
Morphine Sulfate Injection, USP, 50 mg/50 mL (1 mg/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 12th St. Extension, West Columbia, SC 29172, NDC: 69374-979-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1419-2022·2022-07-27
Orthopedic Surgical Guide with Defective Spring Subject to Corrosion
DePuy Orthopaedics is recalling 872 units of the ATTUNE Measured Sizing and Rotation Guide due to a manufacturing defect. A galvanized steel spring was used instead of stainless steel, which may cause corrosion and surgical complications.
Product
ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the femoral implant Part Number: 254400525
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1339-2022·2022-07-27
Dietary Supplement Marketed as Unapproved Drug Recalled by FDA
Launch Sequence Capsules, a dietary supplement sold in 60-count bottles, were recalled because they were marketed without FDA approval as a drug based on label claims.
Product
Launch Sequence Capsules, Dietary Supplement, 60- count bottles, ASIN B07TLPWXDS, UPC Code 641378938375.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1492-2022·2022-07-27
Honeymoon Cinna-Bee Patties recalled due to undeclared tree nuts
Queen Bee Gardens is recalling Honeymoon Cinna-Bee Patties due to potential undeclared tree nuts: pecans, almonds, coconut, macadamia nuts, and walnuts. Products were distributed in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Honeymoon Cinna-Bee Patties. PLU Code: 788394 14892 7
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1476-2022·2022-07-27
Honey Caramels Creamy Fudge Recalled for Undeclared Tree Nuts
Queen Bee Gardens, LLC is recalling Honey Caramels Creamy Fudge because the product may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts). People with tree nut allergies should not consume this product.
Product
Honey Caramels Creamy Fudge. Net wt. 5.87. PLU Code: 788394 12354 2.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1477-2022·2022-07-27
Honey Caramels Huckleberry Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honey Caramels Huckleberry (5.87 oz) because they may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. This poses a serious health risk to people with tree nut allergies.
Product
Honey Caramels Huckleberry. Net wt. 5.87 oz. PLU Code: 788394 12623 9. Ingredients: Honey, butter (pasteurized cream & salt), cream, nonfat dry milk, natural flavors, purple cabbage (coloring), whey, lecithin, algin & agar.
Category
Food
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