State

Pennsylvania product recalls

72,907 recalls have nationwide distribution and so reach Pennsylvania. 11,918 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total: 11,918
Critical: 1,922
Severe: 2,866
Most recent: 2026-09-09

Of the 11,918 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 2,866 (24%) are Severe.

Which agencies issued them

These figures cover only the 11,918 recalls whose distribution notice names Pennsylvania specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1426–1450 of 84825

HighFDA (Devices)·Z-2341-2026·2026-06-17
MIC Safety 7170-14 push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 14 Fr PUSH OTW, catalog number 7170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 22 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2343-2026·2026-06-17
MIC Safety 24 Fr push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 24 Fr PUSH OTW, catalog number 7170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 132 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2322-2026·2026-06-17
TDC VELOCE 23 gauge vitrectomy cutters may have loose outer knife
TDC VELOCE 23G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.
Product
TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2362-2026·2026-06-17
EXENT Analyser marked plates as passed without performing quality control
An EXENT Analyser is being recalled after plates 2 and 3 were marked as passed although quality control appeared not to have been performed, despite samples being measured.
Product
Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2406-2026·2026-06-17
MOSAIQ oncology software may fail to load adapted treatment plan
The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.
Product
MOSAIQ Oncology Information System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2329-2026·2026-06-17
CGuard Prime 10mm by 30mm carotid stents may fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with a 10 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2335-2026·2026-06-17
CORFLO Safety PEG kit 30-6312 contains recalled lidocaine injection
CORFLO Safety PEG Kits, catalog number 30-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 31 kits are affected.
Product
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2399-2026·2026-06-17
Hintermann left talar implant packaging contained a right-side device
Hintermann Series Talar Implants, Left, Size 2, are being recalled because packaging and labeling for a left implant contained a right implant device. 67 units are affected.
Product
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2407-2026·2026-06-17
Halyard pain packs shipped without validated sterilization in Iowa
Halyard Pain Packs, kit code AMPK48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 120 kits affected.
Product
Halyard, Pain Pack. Kit Code: AMPK48-01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2351-2026·2026-06-17
MIC Safety 20 Fr PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits with ENFit Connectors, 20 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues. 6,005 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2346-2026·2026-06-17
MIC Safety 24 Fr pull PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2327-2026·2026-06-17
CGuard Prime 9mm by 30mm carotid stents may fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with a 9 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2348-2026·2026-06-17
MIC Safety 20 Fr push OTW PEG kits contain recalled lidocaine
MIC Safety PEG Kits with ENFit Connectors, 20 Fr PUSH OTW, catalog number 8170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2337-2026·2026-06-17
CORFLO Safety PEG kit 50-4320 contains recalled lidocaine injection
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 49 kits affected.
Product
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2338-2026·2026-06-17
CORFLO Safety PEG kit 50-5320 contains recalled lidocaine injection
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-5320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 72 kits affected.
Product
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2336-2026·2026-06-17
CORFLO Safety PEG kit 30-6316 contains recalled lidocaine injection
CORFLO Safety PEG Kits, catalog number 30-6316, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 41 kits are affected.
Product
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2318-2026·2026-06-17
GE Allia Moveo angiographic systems pose shock risk to service personnel
Allia Moveo angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Three units affected.
Product
Allia Moveo angiographic X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2334-2026·2026-06-17
CORFLO Safety PEG kit 30-5320 contains recalled lidocaine injection
CORFLO Safety PEG Kits, catalog number 30-5320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 61 kits are affected.
Product
Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2325-2026·2026-06-17
CGuard Prime 8mm by 30mm carotid stents may fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2321-2026·2026-06-17
Bicarby dialysate luer-lock connections may leak fluid onto floors
Bicarby Dialysate across six model numbers is being recalled because luer-lock leaks during preparation present a potential slip and fall hazard from fluid on the floor.
Product
Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2345-2026·2026-06-17
MIC Safety 20 Fr pull PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 20 Fr PULL, catalog number 7180-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 3,184 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2402-2026·2026-06-17
Boston Scientific reusable CSK stainless steel electrodes may underperform expected levels
Boston Scientific CSK stainless steel electrodes across several lengths are being recalled because the reusable electrodes may not meet expected performance levels. 31,923 units affected.
Product
Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm) REF: CSK-TC10-3M,CSK Electrode, STAINLESS STEEL, 3M Cable, 10 cm x 28 ga (0.36 mm); REF: CSK-TC15, CSK Electrode, STAINLESS STEEL, 15 cm x 28 ga (0.36 mm); REF: CSK-TC15-3
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2331-2026·2026-06-17
SporeTraq 52-test mail-in spore testing service used incorrect incubation
The SporeTraq Mail-In Spore Testing Service, 52 tests, is being recalled because an incorrect incubation process was performed on the product. 2,210 units are affected.
Product
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Model/Catalog Number: 1023780 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 52 bacterial Spore Strip
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2320-2026·2026-06-17
EXCOR pediatric blood pump valves carry mismatched inner package expiration dates
EXCOR Pediatric VAD System blood pump PU valves are being recalled because the inner package expiration date does not match the correct outer package date.
Product
EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2319-2026·2026-06-17
Mahurkar Elite PASS trays shipped without the labeled Tegaderm CHG dressing
Mahurkar Elite PASS Trays are being recalled because the Tegaderm CHG dressing specified in the product labeling was missing from certain lots. 25,627 units are affected.
Product
Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221413), 12 FR x 16cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222416), 12 FR x 16cm Acute Dual Lumen Catheter wi
Category
Medical Device
Distribution
Distributed nationwide