The Recall Desk

State

Pennsylvania product recalls

73,100 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 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9201–9225 of 85026

  • ModerateFDA (Devices)·Z-0684-2025·2024-12-25

    Eclipse PRO Holter Recorders Recalled for Serial Number Mismatch

    Spacelabs Healthcare recalls 13,202 Eclipse PRO Holter recorders due to manufacturing error where the programmed serial number may not match the physical label. Affected devices were manufactured between April 2021 and November 2024.

    Product
    Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the patient s ambulatory electrocardiogram.
    Category
    Medical Device
    Distribution
    22 states
  • ModerateFDA (Devices)·Z-0685-2025·2024-12-25

    ECG Patch Recorder Serial Number Mismatch - Eclipse Mini

    Spacelabs Healthcare is recalling the Eclipse Mini ECG patch recorder because incorrect serial numbers may be programmed into devices, causing a mismatch between the physical label and internal serial number.

    Product
    Eclipse Mini REF 98900 The Eclipse MINI Model 98900 is a portable non-invasive continuous ambulatory ECG patch recorder intended to record the patient s electrocardiogram.
    Category
    Medical Device
    Distribution
    22 states
  • ModerateFDA (Drugs)·D-0145-2025·2024-12-25

    Topical Anesthetic Gel Recalled for Manufacturing Process Deviation

    Safco SensiCaine Ultra Topical Anesthetic Gel is being recalled due to a manufacturing process deviation. Product that should have been rejected because of damage to the mixing vessel was inadvertently released to customers.

    Product
    SAFCO SENSICAINE ULTRA TOPICAL ANESTHETIC GEL — SAFCO SENSICAINE ULTRA TOPICAL ANESTHETIC GEL (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0691-2025·2024-12-25

    K-Systems R65 embryo incubator temperature may exceed setpoint

    CooperSurgical's K-Systems R65 Trolley reproductive incubators may experience temperature excursions above desired setpoints, though devices will alarm when this occurs. The FDA issued a Class II recall of 43 units across eight U.S. states.

    Product
    Brand Name: K-Systems Product Name: R65 Trolley Model/Catalog Number: K24012 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes and em
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Drugs)·D-0141-2025·2024-12-25

    Patterson Dental Topical Anesthetic Recalled for Manufacturing Quality Defect

    Keystone Industries is recalling one lot of Patterson Dental Topical Anesthetic due to manufacturing quality deviations. The product was shipped despite being marked for rejection due to scratches in the mixing vessel.

    Product
    PATTERSON DENTAL TOPICAL ANESTHETIC — PATTERSON DENTAL TOPICAL ANESTHETIC (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0143-2025·2024-12-25

    Topical anesthetic gel recall due to manufacturing quality control deviation

    Keystone Industries recalls Burkhart Topical Anesthetic Gel due to CGMP deviations discovered during quality inspection. The product was inadvertently released despite being flagged for rejection.

    Product
    Burkhart, Topical Anesthetic Gel, Benzocaine 20%, Gluten Free, 1 FL. OZ (30 ml), Manufactured for Burkhart Dental Supply, Tacoma, Washington 98409.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0148-2025·2024-12-25

    FDA Recalls Benzo-Jel Topical Anesthetic Gel Due to Manufacturing Defect

    Henry Schein's Benzo-Jel Topical Anesthetic Gel is being recalled due to manufacturing quality deviations. Scratches were discovered on the mixing vessel after the product had been inadvertently released and distributed to customers.

    Product
    Henry Schein, Benzo-Jel, Topical Anesthetic Gel, 20% Benzocaine, 1 fl. oz. (29.6 mL), Distributed by Henry Schein, Melville, NY 11747, For Professional Use Only,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0150-2025·2024-12-25

    Dihydroergotamine Mesylate Injection recalled due to discoloration

    Provepharm Inc. is voluntarily recalling Dihydroergotamine Mesylate Injection nationwide due to discoloration in specific lots. Patients should contact their healthcare provider if they have used the affected product.

    Product
    DIHYDROERGOTAMINE MESYLATE — DIHYDROERGOTAMINE MESYLATE (DIHYDROERGOTAMINE MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0147-2025·2024-12-25

    Benzocaine Topical Gel Recalled Due to Manufacturing Quality Defect

    Keystone Industries recalls Ipana 20% Benzocaine Topical Gel due to a manufacturing quality issue. The bulk product was released from a mixing vessel with scratches despite Quality Unit rejection.

    Product
    Ipana, 20% Benzocaine Topical Gel, 28g, Maxill Inc., St Thomas ON Canada.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0137-2025·2024-12-25

    Benzocaine Topical Anesthetic Recalled for Manufacturing Equipment Defect

    Gelato Benzocaine 20% topical anesthetic (Lot BNZ-001646) is recalled due to scratches found in the mixing vessel during manufacturing. The defective product was inadvertently released despite quality control rejection, though no illnesses have been reported.

    Product
    GELATO TOPICAL ANESTHETIC — GELATO TOPICAL ANESTHETIC (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0154-2025·2024-12-25

    Olanzapine 2.5 mg Tablets Recalled for Failed Impurity Specifications

    Macleods Pharmaceuticals is recalling Olanzapine 2.5 mg tablets nationwide due to failed impurities and degradation specifications. The recall affects one production lot distributed across the United States.

    Product
    OLANZAPINE — OLANZAPINE (OLANZAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V966000·2024-12-23

    Storyteller Overland Recalls 2024 Vehicles Due to Alternator Fire Risk

    Storyteller Overland is recalling 196 2024 vehicles because an improperly torqued alternator component may overheat and cause a fire.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND MYSTIC, CLASSIC, STEALTH, BEAST MODE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V968000·2024-12-23

    Storyteller Overland Recalls 2023-2024 GXV HILT Vehicles for Grounding Defect

    Storyteller Overland is recalling 2023-2024 GXV HILT vehicles because improperly grounded metal frames may cause electric shock. Dealers will install bonding wires free of charge.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND GXV HILT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V969000·2024-12-23

    Nissan Kicks shift-to-park warning may not activate as intended

    Nissan is recalling certain 2025 Kicks vehicles because the shift-to-park warning may not activate when the vehicle is shut off while still in gear, failing FMVSS 114.

    Product
    NISSAN — NISSAN KICKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V970000·2024-12-23

    Indian Scout gear position display may falsely show neutral

    Indian Motorcycle is recalling certain 2025 Scout and Scout Sixty motorcycles because the gear position display may falsely show that the motorcycle is in neutral.

    Product
    INDIAN — INDIAN SCOUT, SCOUT SIXTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V954000·2024-12-20

    Ford Escape high voltage battery cells may short circuit internally

    Ford is recalling certain 2020-2024 Escape and 2021-2024 Lincoln Corsair vehicles because a manufacturing defect in high voltage battery cells may cause an internal short circuit.

    Product
    FORD — FORD, LINCOLN ESCAPE, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V952000·2024-12-20

    Altec AT200A Front Axle Defect Recall for Ford E350 Chassis

    Altec is recalling AT200A devices on 2017-2024 Ford E350 chassis due to a front axle defect that may fail at high loads, increasing injury risk.

    Product
    ALTEC — ALTEC AT200A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V960000·2024-12-20

    Mercedes-Benz Recalls 2023 EQS 450+ for Air Bag Bracket Defect

    Mercedes-Benz is recalling 2023 EQS 450+ vehicles because sharp edges on roof mounting brackets may damage side-curtain air bags during deployment, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 450+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS· 034-2024·2024-12-20

    Impero Foods Recalls Raw Pork Sausage Produced Without Federal Inspection

    Impero Foods & Meats, Inc. is recalling approximately 7,485 pounds of raw pork sausage produced without federal inspection. The products were distributed to restaurants and retailers in Delaware, Maryland, and Pennsylvania.

    Product
    Impero Foods & Meats, Inc. — Impero Foods & Meats, Inc. Recalls Raw Pork Sausage Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·24V851000·2024-12-20

    Ford F-150 misaligned engine cup plugs may cause rapid oil leaks

    Ford is recalling certain 2024-2025 F-150, 2024 Expedition and Lincoln Navigator vehicles with 3.5L GTDI engines because a misaligned engine cup plug can cause a rapid oil leak.

    Product
    LINCOLN — LINCOLN, FORD NAVIGATOR, EXPEDITION, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide