State

Pennsylvania product recalls

72,820 recalls have nationwide distribution and so reach Pennsylvania. 11,910 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total: 11,910
Critical: 1,922
Severe: 2,864
Most recent: 2026-09-02

Of the 11,910 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 2,864 (24%) are Severe.

Which agencies issued them

These figures cover only the 11,910 recalls whose distribution notice names Pennsylvania specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

251–275 of 84730

SevereFDA (Drugs)·D-0762-2026·2026-08-19
Shoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
Shoolin Pharma Chem LLP is recalling Tadalafil USP 1.00 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Product
TADALAFIL USP, 1.00 KG, 1KG(1000gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO 171596-29-5), NDC 85702-001-08
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0754-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 250 vials of Semaglutide 5mg due to the presence of nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.NDC 71170-712-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0753-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 250 vials of Semaglutide 2.5mg due to the presence of nylon and silk particulate matter.
Product
SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0757-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling specific lots of Semaglutide 20mg vials because they contain nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-724-04.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0756-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 500 vials of Semaglutide 10mg due to the presence of nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0749-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling specific lots of Semaglutide 6.75mg vials because they contain nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0752-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.
Product
SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0755-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care is recalling 250 vials of Semaglutide 7.5mg due to the presence of nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0748-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling specific lots of Semaglutide 2.25mg vials because they contain nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0747-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 56,918 vials of Semaglutide 12.5mg due to the presence of nylon and silk particulate matter.
Product
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1288-2026·2026-08-19
Taylor Farms Recalls Cross Valley Farms Lettuce Due to Cyclospora Risk
Taylor Farms is recalling specific Cross Valley Farms lettuce products due to potential Cyclospora contamination. Consumers should check lot codes and discard or return affected items.
Product
Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-2936-2026·2026-08-19
BioFire Respiratory Panel 2.1 Recalled for Increased False Negative Results
BioFire Diagnostics is recalling 2,370 pouches of the BIOFIRE Respiratory Panel 2.1 test due to an increase in false negative results.
Product
BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2926-2026·2026-08-19
Medline Micro-Kill Bleach Germicidal Wipes Recalled for Reduced Concentration
Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because bleach concentration may drop below specification, potentially compromising disinfection effectiveness.
Product
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2943-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Product
Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V537000·2026-08-19
E-One Recalls Fire Trucks Due to Hydraulic Valve Defect
E-One is recalling specific 2025-2026 fire trucks because a hydraulic valve defect may prevent outriggers from extending or retracting, potentially delaying emergency response.
Product
E-ONE — E-ONE CYCLONE N, CYCLONE II, TYPHOON N
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2928-2026·2026-08-19
Philips Allura Xper FD Fluoroscopic X-Ray System Recalled for Firmware Issue
Philips is recalling 4,252 Allura Xper FD interventional fluoroscopic x-ray systems worldwide due to a firmware issue that may cause loss of geometry movements.
Product
Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2918-2026·2026-08-19
V-Loc 90 Absorbable Wound Closure Devices Recalled for Packaging Defects
Covidien, LP is recalling V-Loc 90 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that may cause biocontamination.
Product
V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 GS-25 VLOCM0436 VLOCM0436 VLOCM0003 V-LOC* 90 4-0 CLR 15CM P12X12 VLOCM0003 VLOCM0013 V-LOC* 90 4-0 CLR 30CM P12X12 VLOCM0013 VLOCM0024 V-LOC* 90 3-0 CLR 45CM P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2947-2026·2026-08-19
Cardinal Health Recalls Neurological Procedure Kits Due to Endotoxin Variability
Cardinal Health is recalling specific Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Product
Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC27; 2) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC28; 3) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC2C; 4) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2924-2026·2026-08-19
Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness
Medline is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness, potentially allowing pathogenic microorganisms to survive.
Product
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0751-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling specific lots of Semaglutide 9mg vials because they contain nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2948-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
Cardinal Health 200, LLC is recalling 52,699 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.
Product
Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH5; 4) KIT, ANT CERVICAL DISC , Catalog Number: PN41
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2945-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Product
Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog Number: PE13SPAJB; 4) KIT, SINUS , Catalog Number: PE13SPAJC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2921-2026·2026-08-19
Surgipro Sutures Recalled for Potential Sterile Barrier Perforation
FDA is recalling Surgipro sutures due to potential sterile barrier defects that could cause biocontamination and infection.
Product
Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26E059000·2026-08-19
Avride Recalls Automated Driving Systems Due to Unsafe Lane Changes
Avride Inc. is recalling Automated Driving Systems (ADS) with specific software versions that may cause unsafe lane changes or merging without yielding.
Product
ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2923-2026·2026-08-19
Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness
Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness.
Product
Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8", 150 count, 150 count, Product Number MSC351400AN
Category
Medical Device
Distribution
Distributed nationwide