State

Pennsylvania product recalls

73,092 recalls have nationwide distribution and so reach Pennsylvania. 11,926 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total: 11,926
Critical: 1,922
Severe: 2,869
Most recent: 2026-09-25

Of the 11,926 recalls naming Pennsylvania we have scored against our rubric, 1,922 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,869 (24%) are Severe.

Which agencies issued them

These figures cover only the 11,926 recalls whose distribution notice names Pennsylvania specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7826–7850 of 85018

HighFDA (Food)·F-0683-2025·2025-04-09
Lean Cuisine Ravioli Recalled Due to Potential Wood-Like Foreign Material
Nestle USA is recalling Lean Cuisine Spinach Artichoke Ravioli due to potential wood-like foreign material in the product. The affected 9-ounce frozen meals were distributed across 33 states.
Product
Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1477-2025·2025-04-09
Hemopore nasal wound dressing packaging seal defect may compromise sterility
Stryker Corporation is recalling 182,344 units of Hemopore nasal/sinus wound dressing due to potential packaging seal defects that could compromise sterility. A bubble on the blister seal may indicate the sterile barrier has been breached.
Product
Hemopore 8cm nasal/sinus temporary wound dressing, Catalog Numbers 5400-020-208 and 5400-020-208ITL (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2025·2025-04-09
Stryker nasal wound dressing recalled for defective sterile packaging seal
Stryker Corporation is recalling 182,344 units of Hemopore 2PK nasal/sinus wound dressing due to potential bubbles in blister seals that indicate sterility breach. Affected lot numbers are 2024020221, 2024051720, and 2024082321.
Product
Hemopore 2PK nasal/sinus temporary wound dressing, Catalog Number 5400-222-208S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0719-2025·2025-04-09
Chocolate Spread Recalled: CACAO BARRY Gianduja Noir Contains Undeclared Milk
CACAO BARRY Gianduja Noir chocolate product is recalled due to undeclared milk, affecting 180 cases distributed across eight states. Consumers with milk allergies should not consume this product.
Product
CACAO BARRY Gianduja Noir, 5.5lbs (2.5kg) plastic bucket, 8 buckets per case.
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1472-2025·2025-04-09
Otopore Cylinder Wound Dressing Recalled for Potential Sterility Seal Defect
Stryker Corporation recalls Otopore Cylinder outer ear wound dressing due to potential bubbles in blister seals that may breach the sterile barrier. Affected units were distributed nationwide.
Product
Otopore Cylinder outer ear wound dressing, Firm Catalog Number 5400-020-000 and Forte Catalog Number 5400-020-000TL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0308-2025·2025-04-09
Prescription Duloxetine Capsules Recalled for Nitrosamine Impurity
Breckenridge Pharmaceutical is recalling Duloxetine 30 mg capsules distributed nationwide due to a nitrosamine impurity above acceptable limits. Consumers should consult their doctor about their medication.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1470-2025·2025-04-09
Nasopore nasal dressing may have compromised sterile packaging
Stryker is recalling Nasopore Standard 4cm nasal dressings because the blister seals may develop bubbles, potentially compromising the sterility barrier. Affected units should not be used.
Product
Nasopore Standard 4cm fragmentable nasal dressing, Catalog Numbers 5400-010-004 and 5400-010-004ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1501-2025·2025-04-09
Phoroptor VRx Digital Refraction System Recalled for Detachable Head
Reichert is recalling 1,876 units of the Phoroptor VRx Digital Refraction System (Model 16242) due to an assembly defect that could cause the refraction head to detach during eye examinations.
Product
Phoroptor VRx Digital Refraction System Model Numbers: 16242
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25E025000·2025-04-09
Hiab Recalls Waltco ZS-MK2 Lift Gates Due to Pin Seizure Risk
Hiab USA Inc. is recalling specific Waltco ZS-MK2 series lift gates because insufficient lubrication may cause the cylinder pin to seize, leading to lift gate failure and injury risk.
Product
STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1475-2025·2025-04-09
Otopore Square Outer Ear Wound Dressing Recall for Sterility Seal Defect
Stryker Corporation is recalling Otopore Square outer ear wound dressings nationwide because sterile packaging seals may develop bubbles, indicating a potential breach of the sterile barrier. Consumers should stop using affected units and contact their healthcare provider.
Product
Otopore Square outer ear wound dressing, Firm Catalog Number 5400-020-100 and Forte Catalog Number 5400-020-100ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2025·2025-04-09
Surgical Suture Recall Due to Silicone Curing Defect
Ethicon Endo Surgery recalls ETHIBOND EXCEL surgical sutures worldwide due to curing issues with the silicone coating on the needles identified during manufacturing.
Product
ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1481-2025·2025-04-09
Nasopore Nasal Dressings Recalled Due to Breached Sterility Seals
Stryker Corporation is recalling Nasopore nasal dressings due to potential breaches in packaging sterility seals that could compromise product sterilization. Approximately 182,344 units have been distributed nationwide.
Product
Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1471-2025·2025-04-09
Nasopore Standard Nasal Dressing Recalled Due to Sterility Seal Defects
Stryker is recalling 182,344 units of Nasopore Standard nasal dressings nationwide due to potential bubbles in blister seals that may breach the sterility barrier and increase contamination risk.
Product
Nasopore Standard 8cm fragmentable nasal dressing, Catalog Numbers 5400-010-008 and 5400-010-008ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1490-2025·2025-04-09
Stryker Spine Monterey AL Implant Inserter Recall Due to Potential Gold Button Separation
Stryker Spine is recalling the Monterey AL Implant Inserter because the gold unlock button may separate from the device, which could affect functionality during surgical procedures.
Product
Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1469-2025·2025-04-09
Otopore Outer Ear Dressings Recalled for Compromised Sterile Packaging Seals
Stryker Corporation is recalling 182,344 Otopore Cylinder Standard outer ear dressings due to potential defects in blister seals that may compromise sterility. Bubbles in packaging seals indicate the sterile barrier is breached.
Product
Otopore Cylinder Standard outer ear dressings, Catalog Numbers 5400-010-000 and 5400-010-000ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0682-2025·2025-04-09
Lean Cuisine Butternut Squash Ravioli Recalled for Potential Foreign Material
Nestle-USA recalls Lean Cuisine Butternut Squash Ravioli for potential wood-like foreign material. Approximately 50,611 cases distributed across 36 states are affected.
Product
Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
Category
Food
Distribution
37 states
HighNHTSA·25V225000·2025-04-09
Audi Q6 e-tron rearview cameras may show a blurry image
Volkswagen is recalling certain 2025 Audi Q6 e-tron and SQ6 e-tron vehicles because the rearview camera may show a blurry image, failing FMVSS 111.
Product
AUDI — AUDI Q6 E-TRON, SQ6 SPORTBACK E-TRON
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1473-2025·2025-04-09
Stryker Nasopore Nasal Dressing Recalled for Compromised Sterility Seals
Stryker's Nasopore 8cm nasal dressing is being recalled because packaging seals may have bubbles indicating the sterility barrier has been breached. The recall affects 182,344 units distributed nationwide.
Product
Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0681-2025·2025-04-09
Lean Cuisine Lemon Garlic Shrimp Stir Fry Recalled Due to Foreign Material
Nestle-USA recalls Lean Cuisine Lemon Garlic Shrimp Stir Fry (10 oz) due to potential wood-like foreign material. Approximately 7,212 cases distributed across 37 states; check Batch Number 4214595511 (Best By September 2025).
Product
Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a paperboard carton; 10 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1491-2025·2025-04-09
Stryker Spine Monterey AL Implant Inserter Recalled for Potential Unlock Button Separation
Stryker Spine is recalling the Monterey AL Implant Inserter (22mm, Catalog 48019140) due to potential separation of the gold unlock button from the device. The recall affects 41 units in the United States and 3 internationally.
Product
Monterey AL Implant Inserter; 22mm; Catalog 48019140.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1474-2025·2025-04-09
Nasopore nasal dressing recall: compromised sterile barrier seals
Stryker recalls Nasopore 4cm fragmentable nasal dressings due to potential blister seal damage that compromises the sterile barrier. Nationwide distribution affected.
Product
Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1488-2025·2025-04-09
Stryker Monterey AL Implant Inserter Gold Button Detachment Risk
Stryker Spine is recalling Monterey AL Implant Inserters due to a potential defect where the gold unlock button may separate from the device, compromising its function during spinal surgery.
Product
Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1509-2025·2025-04-09
BD Connecta Stopcocks Recalled for Non-U.S. Instructions Shipped to U.S. Market
BD Connecta Luer-Lok 360 stopcocks were distributed with non-U.S. instructions for use. Healthcare facilities should verify they have the correct U.S. instructions before using affected lot numbers.
Product
BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressure monitoring.
Category
Medical Device
Distribution
35 states
HighNHTSA·25V226000·2025-04-09
Audi Q6 rearview camera image may be delayed or deactivated
Volkswagen is recalling certain 2025 Audi Q6 and SQ6 vehicles because the rearview camera image may be delayed or deactivated after shifting into reverse, failing FMVSS 111.
Product
AUDI — AUDI SQ6 SPORTBACK E-TRON, Q6 E-TRON
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1503-2025·2025-04-09
Laboratory diagnostic reagent distributed with incorrect calibration value on package label
Fisher Diagnostics is recalling Pacific Hemostasis Thromboplastin-D reagent (1,699 units) due to an incorrect International Sensitivity Index (ISI) value printed on the box. No illnesses or injuries have been reported.
Product
Pacific Hemostasis Thromboplastin-D, 10 ml. Used in performing one-stage prothrombin time test and factor assays.
Category
Medical Device
Distribution
1 state