State

Pennsylvania product recalls

73,576 recalls have nationwide distribution and so reach Pennsylvania. 11,931 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total: 11,931
Critical: 1,922
Severe: 3,380
Most recent: 2026-10-14

Of the 11,931 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 3,380 (28%) are Severe.

Which agencies issued them

These figures cover only the 11,931 recalls whose distribution notice names Pennsylvania specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24401–24425 of 85507

SevereFDA (Food)·F-0970-2022·2022-04-13
Watermelon Products Recalled Due to Potential Listeria Contamination
Fruit Fresh Up, Inc. recalled watermelon products from multiple retailers due to potential Listeria monocytogenes contamination. The recall affects 39,232 units distributed in NY, MA, and PA with best-by dates of March 5–23, 2022.
Product
1. Wegmans 10oz Watermelon Chunks 2. Wegmans 32oz Watermelon Chunks 3.Fresh Harvest 18oz Watermelon Chunks 4. Tops Large Watermelon BBD: 3/5/22 to BBD: 3/22/22 5. Tops Small Watermelon BBD: 3/5/22 to BBD: 3/22/22 6. Lexington Co-op 10oz Watermelon Chunks 7. Lexington…
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0973-2022·2022-04-13
Multiple cantaloupe products recalled due to potential Listeria contamination
Fruit Fresh Up, Inc. is recalling six cantaloupe products distributed in NY, MA, and PA (39,232 units) due to potential Listeria monocytogenes contamination. Products have best-by dates between March 5 and March 26, 2022.
Product
All BBD 03/05/22 through 03/23/2022 1. Wegmans 32oz Cantaloupe Spears 2. Fresh Harvest 18oz Cantaloupe Spears 3. Tops Large Cantaloupe 4. Tops Small Cantaloupe 5. Lexington Co-op 10oz Cantaloupe Chunk (4/cs) 6. EDU Kids 2 oz. Cantaloupe tidbits
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0972-2022·2022-04-13
Fruit Fresh Up melon trio and combo products recalled for Listeria contamination
Melon trio and combo products from Fruit Fresh Up may contain Listeria monocytogenes. Products distributed in NY, MA, and PA with best-by dates from March 5–23, 2022 are affected.
Product
1. Wegmans 32oz Melon Trio 2.Fresh Harvest 18oz Melon Trio 64779300400 3. Lexington Co-op 32oz Melon Trios 64779300403 4. Lexington Co-op 10oz Melon Combo 64779300370 5. Tops Large Mixed Melon 6. Tops Small Mixed Melon
Category
Food
Distribution
3 states
SevereNHTSA·22V241000·2022-04-13
New England Wheels Recalls 2021-2022 Frontrunner Buses for Fire Risk
New England Wheels is recalling 2021-2022 Frontrunner buses because a faulty module may cause a fire. Owners should contact the manufacturer for a free repair.
Product
NEW ENGLAND WHEELS — NEW ENGLAND WHEELS FRONTRUNNER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0977-2022·2022-04-13
Fruit Fresh Up Raspberry Dip Recalled Due to Listeria Contamination Risk
Fruit Fresh Up, Inc. is recalling Fruit Fresh Up Raspberry Dip (7oz) due to potential Listeria monocytogenes contamination. Affected units distributed in NY, MA, and PA should not be consumed.
Product
Fruit Fresh Up Raspberry Dip (7oz)
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0981-2022·2022-04-13
Doodlebugs Tidbits Mix Recalled Due to Potential Listeria Contamination
Fruit Fresh Up, Inc. is recalling Doodlebugs Tidbits Mix (cantaloupe, honeydew, pineapple, watermelon) distributed in New York, Massachusetts, and Pennsylvania due to potential Listeria monocytogenes contamination.
Product
Doodlebugs 12 # Tidbits Mix (cantaloupe, honeydew, pineapple, watermelon )
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0978-2022·2022-04-13
Fruit Fresh Up Recalls Bulk Fruit Salad for Potential Listeria Contamination
Fruit Fresh Up, Inc. is recalling Eden Valley Bulk Fruit Salad which may be contaminated with Listeria monocytogenes. The recall affects 39,232 units distributed in New York, Massachusetts, and Pennsylvania.
Product
Eden Valley Bulk Fruit Salad
Category
Food
Distribution
3 states
SevereNHTSA·22E032000·2022-04-13
NTN Driveshaft Recall: Improper Heat Treatment May Cause Failure
NTN Bearing Corporation is recalling specific driveshafts because internal components may not have been heat-treated properly. This defect could lead to driveshaft failure and a sudden loss of drive power.
Product
POWER TRAIN:DRIVELINE:DRIVESHAFT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0763-2022·2022-04-13
FDA Recalls SYMJEPI Epinephrine Injection for Potential Needle Clogging
Adamis Pharmaceuticals is recalling SYMJEPI epinephrine injections due to potential needle clogging that may prevent medication delivery. The FDA has classified this as a Class I recall affecting nationwide distribution.
Product
SYMJEPI (epinephrine injection, USP) 0.3 mg, (0.3 mg/0.3 mL), Two Pre-Filled Single-Dose Syringes per carton, Rx Only, Manufactured for Adamis Pharmaceuticals Corp.; San Diego, CA 92130; Distributed by USWM, LLC., Louisville, KY 40241, Made in Belgium, NDC 78670-130-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0975-2022·2022-04-13
Fresh Harvest veggie platter recalled for possible Listeria contamination
Fruit Fresh Up, Inc. is recalling Fresh Harvest Small veggie platters with ranch that may be contaminated with Listeria monocytogenes. Affected products were distributed in New York, Massachusetts, and Pennsylvania.
Product
Fresh Harvest Small veggie platter w/ranch 64779300337
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0979-2022·2022-04-13
Tops Dill Dip Bulk recalled due to Listeria contamination risk
Tops Dill Dip Bulk is being recalled due to potential contamination with Listeria monocytogenes. Consumers should stop using the product and dispose of it safely.
Product
Tops Dill Dip Bulk
Category
Food
Distribution
3 states
SevereFDA (Drugs)·D-0764-2022·2022-04-13
SYMJEPI Epinephrine Injection Recalled for Defective Delivery System Nationwide
Adamis Pharmaceuticals is recalling 2,500 cartons of SYMJEPI (epinephrine injection) nationwide due to a defective delivery system that may clog the needle and prevent medication dispensing.
Product
SYMJEPI (epinephrine injection, USP) 0.15 mg (0.15 mg/0.3 mL), Two Pre-Filled Single-Dose Syringes per carton, Rx Only, Manufactured for Adamis Pharmaceuticals Corp.; San Diego, CA 92130; Distributed by USWM, LLC., Louisville, KY 40241, Made in Belgium, NDC 78670-131-02.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0980-2022·2022-04-13
MapleVale 18# Wet Salad Bucket Recalled for Listeria Contamination
Fruit Fresh Up, Inc. recalls MapleVale 18# Wet Salad Bucket due to potential Listeria monocytogenes contamination. Affected products were distributed in New York, Massachusetts, and Pennsylvania.
Product
MapleVale 18# Wet Salad Bucket Cut Cantaloupe, Honeydew, Pineapple, Grapes in Watermelon Juice with Potassium sorbate added.
Category
Food
Distribution
3 states
SevereNHTSA·22V238000·2022-04-13
Lexus Recalls 2022 NX Models for Front Shock Absorber Weld Defect
Lexus is recalling 2022 NX250, NX350, NX350h, and NX450h+ vehicles because missing spot-welds may cause the front shock absorber to separate, increasing crash risk.
Product
LEXUS — LEXUS NX350H, NX250, NX450H+, NX350
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0759-2022·2022-04-13
Pfizer Recalls Blood Pressure Tablets Due to Manufacturing Defects
Pfizer is recalling quinapril HCl/hydrochlorothiazide tablets due to manufacturing defects that allowed N-nitroso impurities to exceed acceptable daily intake limits. Patients taking affected lots should contact their pharmacy.
Product
quinapril HCl/hydrochlorothiazide tablets, 20 mg/12.5 mg*, 90 Tablets bottles, Rx Only, Distributed by: Greenstone, LLC, Peapack, NJ, 07977, Made in Germany, NDC 59762-0220-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0865-2022·2022-04-13
Anterior Hip Surgical Kit Recall Due to Potential Sterility Breach
Stradis Medical is recalling Anterior Hip Pack surgical kits due to perforated or torn outer bags that may compromise sterility. No illnesses have been reported.
Product
Anterior Hip Pack - Surgical Kit
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V240000·2022-04-13
2022-2023 BMW iX Air Bag Warning System Software Defect
BMW is recalling 2022-2023 iX vehicles due to incorrect software in the air bag control unit. The malfunction indicator light may not illuminate if the air bag system has a problem, increasing crash injury risk.
Product
BMW — BMW IX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0963-2022·2022-04-13
Caesar Dressing in 1.5 oz Pouch Recalled for Undeclared Soy Allergen
Caesar dressing in 1.5 oz pouches manufactured by Sauer Brands Inc is being recalled due to undeclared soy. The product was distributed to institutional foodservice accounts in 14 states and poses a risk to people with soy allergies.
Product
Caesar dressing in a 1.5 oz pouch
Category
Food
Distribution
14 states
HighNHTSA·22V239000·2022-04-13
Electronic Stability Control Software Defect in 2022 Toyota RAV4 Prime and Other Models
Certain Toyota and Lexus vehicles may have a software defect preventing the Electronic Stability Control system from re-engaging after being manually disabled. Dealers will update the software free of charge.
Product
TOYOTA — TOYOTA, LEXUS SIENNA HYBRID, VENZA HYBRID, MIRAI, redundant VENZA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0887-2022·2022-04-13
Surgical drive mechanism recalled due to corrosion risk
Maquet Cardiovascular is recalling the Ultima Activator II Reusable Drive Mechanism due to potential corrosion on pins, which could cause allergic reactions, metal toxicity, and other delayed health effects.
Product
Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
Category
Medical Device
Distribution
14 states
HighFDA (Drugs)·D-0754-2022·2022-04-13
Pfizer recalls Accuretic blood pressure tablets for impurities exceeding acceptable limits
Pfizer is recalling 53 bottles of Accuretic blood pressure tablets nationwide due to manufacturing impurities that exceed FDA acceptable daily intake limits. The affected lot is FG5379, expiring August 2024.
Product
Accuretic (quinapril HCl/hydrochlorothiazide) Tablets, 10 mg/12.5 mg*, 90 Tablets bottles, Rx Only, Distributed by: Parke-Davis, Division of Pfizer Inc, NY, NY 10017, Made in Germany, NDC 0071-3112-23.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V244000·2022-04-13
Nissan Recalls 2020 Sentra Vehicles for Headlight Misalignment
Nissan is recalling 2020 Sentra vehicles with LED headlights because the right-hand headlight may be misaligned, potentially reducing visibility and increasing crash risk.
Product
NISSAN — NISSAN SENTRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0746-2022·2022-04-13
Diabetes Drug Janumet Recalled Due to Stainless Steel Contamination
Merck is recalling 3,600 cartons of Janumet (sitagliptin/metformin HCl) tablets nationwide due to the presence of stainless steel particulates in the tablets.
Product
JANUMET — JANUMET (SITAGLIPTIN AND METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V242000·2022-04-13
2022 Crossroads Zinger Travel Trailers Recalled for Missing Furnace Vent
Keystone RV is recalling 2022 Crossroads Zinger travel trailers because the furnace vent extension may not have been installed. A missing vent can allow carbon monoxide to enter the living area.
Product
CROSSROADS — CROSSROADS ZINGER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0881-2022·2022-04-13
Philips HeartStart HS1 AED Pads: Potential Gel Separation Defect
Philips is recalling adult Smart PADS cartridges for HeartStart HS1 defibrillators due to potential gel separation from the pad backing. Affected pads may have reduced gel contact, potentially affecting device performance.
Product
Philips, REF M5071A, Adult. Smart PADS CARTRIDGE, 8+ years FOR USE WITH HEARSTART HS1 DEFIBRILLATORS
Category
Medical Device
Distribution
Distributed nationwide