The Recall Desk

State

Pennsylvania product recalls

73,503 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 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21801–21825 of 85434

  • SevereCPSC·22227·2022-09-22

    Spalding Momentous EZ Portable Basketball Goals Recalled for Impact Injury Risk

    Russell Brands is recalling about 13,400 Spalding Momentous EZ Portable Basketball Goals because welds in the arm attaching the backboard to the pole can fail, causing the backboard to fall and strike users. The firm has received 26 reports of weld failures and 2 injury reports.

    Product
    Spalding Momentous EZ Portable Basketball Goals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22777·2022-09-22

    Canyon Furniture Ladders Recalled for Entrapment and Strangulation Hazards

    Canyon Furniture Company is recalling approximately 2,100 ladders sold with Canyon Lake and Cottage Colors bunk bed and hutch sets due to a gap wider than 3.5 inches between the fourth ladder step and the hutch cross-member that poses entrapment and strangulation hazards. No injuries have been reported.

    Product
    Ladders sold with Canyon Lake and Cottage Colors Bunk Bed and Hutch Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22773·2022-09-22

    Pool and Spa Drain Covers Recalled for Entrapment Hazard

    Chyir Myd pool and spa drain covers do not meet federal entrapment-protection standards and pose a hazard to swimmers. About 300 units were sold on Amazon from September 2021 through June 2022.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V708000·2022-09-22

    2023 Cadillac XT6, XT5, and GMC Acadia: illegible tire certification label

    General Motors is recalling 2023 Cadillac XT6, XT5, and GMC Acadia vehicles due to illegible tire size information on the driver's side certification label. The illegibility may result in incorrect tires being installed, increasing crash risk.

    Product
    CADILLAC — CADILLAC, GMC XT6, XT5, ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22776·2022-09-22

    Pool and Spa Drain Covers Recalled for Entrapment Hazard

    Angzhili pool and spa drain covers do not meet the Virginia Graeme Baker Pool and Spa Safety Act entrapment protection standards, posing a risk to swimmers and bathers. About 1,000 units sold on Amazon from June 2021 through June 2022 are affected.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V709000·2022-09-22

    2020-2021 GMC Acadia rearview camera may fail due to improper connector crimping

    General Motors is recalling certain 2020-2021 GMC Acadia vehicles with defective rearview camera coaxial cables that may fail or malfunction. The improperly crimped connectors can reduce rear visibility and increase crash risk.

    Product
    CADILLAC — CADILLAC, GMC XT5, XT6, ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22775·2022-09-22

    Pool and Spa Drain Covers Recalled for Entrapment Hazard

    Goetas pool and spa drain covers do not meet the Virginia Graeme Baker Pool and Spa Safety Act standards, creating an entrapment hazard for swimmers and bathers. About 300 units were sold on Amazon from October 2021 through April 2022.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V713000·2022-09-22

    Osage Recalls 2022 Warrior Emergency Vehicles Due to Lighting Failure Risk

    Osage Industries is recalling 2022 Warrior and Super Warrior emergency vehicles because a defective circuit board can cause vehicle lighting to fail, increasing crash risk.

    Product
    OSAGE — OSAGE WARRIOR, SUPER WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V710000·2022-09-22

    2023 Cadillac LYRIQ Instrument Panel Software Error May Cause Display to Go Blank

    General Motors is recalling certain 2023 Cadillac LYRIQ vehicles due to a software error that may cause the instrument panel display to go blank, potentially preventing drivers from seeing critical safety information.

    Product
    CADILLAC — CADILLAC redundant LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V712000·2022-09-22

    2022 Subaru Outback Windshield Defect May Cause Detachment in Crash

    Subaru is recalling 42 2022 Outback and Impreza vehicles due to incorrect paint clearcoat that may insufficiently bond the windshield. The windshield could detach during a crash, increasing injury risk.

    Product
    SUBARU — SUBARU OUTBACK, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22774·2022-09-22

    Wadoy pool and spa drain covers recalled for entrapment hazard

    Find4Fix has recalled about 5,500 Wadoy eight-inch pool and spa drain covers sold on Amazon from August 2019 through June 2022 because they do not meet Virginia Graeme Baker Pool and Spa Safety Act entrapment protection standards.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22228·2022-09-22

    Accompany USA Ceramic Mugs with Cork Bottoms Recall Due to Burn Hazard

    Accompany USA is recalling about 25,000 ceramic mugs with cork bottoms because they can crack or break when hot liquid is poured into them, posing a burn hazard. One incident of breakage has been reported with no injuries.

    Product
    Ceramic Mugs with Cork Bottoms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22226·2022-09-22

    Miffy First LED Lights Recalled for Overheat Burn Hazard

    About 1,400 Miffy First LED Lights can overheat during use, posing a burn hazard. No injuries have been reported. Consumers should stop using the lights and contact the company for a free module replacement.

    Product
    Miffy First LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1540-2022·2022-09-21

    Propofol Injectable Emulsion Recalled for Particulate Matter Contamination

    Pfizer is recalling 5,390 vials of Propofol Injectable Emulsion due to the presence of particulate matter. The affected lot (EA7470, expiration 6/1/2023) was distributed nationwide.

    Product
    PROPOFOL — PROPOFOL (PROPOFOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1504-2022·2022-09-21

    Meijer Magnesium Citrate Laxative Recalled for Microbial Contamination

    Meijer brand magnesium citrate laxative (10 fl oz) has been recalled nationwide due to microbial contamination of Lot 0557622. Consumers should discard or return the product.

    Product
    meijer, magnesium citrate Saline Laxative, Oral Solution, (1.745 g/fl oz), Lemon Flavor, 10 FL OZ (296 mL), Dist. By Meijer Distribution, Inc. Grand Rapids, MI 49544; NDC 41250-708-38 UPC 7 13733 45945 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1506-2022·2022-09-21

    FDA Recalls Citroma Magnesium Citrate Laxative for Microbial Contamination

    Citroma magnesium citrate laxative is recalled due to microbial contamination. The FDA Class I recall affects 42,912 bottles distributed in the USA, Canada, and Panama.

    Product
    CITROMA — CITROMA (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1500-2022·2022-09-21

    CVS Health Magnesium Citrate Saline Laxative recalled for microbial contamination

    CVS Health Magnesium Citrate Saline Laxative is being recalled due to potential microbial contamination of the non-sterile product. Approximately 241,086 bottles were distributed nationwide.

    Product
    CVS Health, Magnesium Citrate SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Lemon Flavor, 10 FL OZ (296 mL), a) UPC 0 50428 30594 2; b) UPC 0 50428 33517 8; Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1509-2022·2022-09-21

    Walgreens Dye-Free Magnesium Citrate Laxative Recalled for Microbial Contamination

    Vi-Jon, LLC is recalling Walgreens Dye-Free Magnesium Citrate Saline Laxative due to microbial contamination of the non-sterile product. Approximately 29,172 bottles distributed nationwide in the USA, Canada, and Panama are affected.

    Product
    Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Lemon Flavor, 10 FL OZ (296 mL), Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-8166-38 UPC 3 11917 20160 3 (green label)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1653-2022·2022-09-21

    Baxter CLEARLINK System Non-DEHP Solution Set recalled due to leak reports

    Baxter Healthcare Corporation is recalling the CLEARLINK System Non-DEHP Solution Set nationwide due to increased customer reports of leaks in the in-line injection site device.

    Product
    Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0212-2024·2022-09-21

    Banana Boat Clear Sunscreen Spray recalled for benzene contamination

    Edgewell Personal Care Brands is recalling Banana Boat hair & scalp defense Clear Sunscreen Spray SPF 30 due to benzene contamination. The affected product was distributed nationwide in the United States.

    Product
    Banana Boat hair & scalp defense, Clear Sunscreen Spray SPF 30, Avobenzone 2.0%, Homosalate 6.0%, Octocrylene 6.0%, packaged in Net Wt 6 oz. aluminum spray can, Distributed by: Edgewell Personal Care Brands, LLC, Shelton, CT 06484, UPC 0 79656 04041 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1505-2022·2022-09-21

    Magnesium Citrate Laxative Recalled Due to Microbial Contamination

    Vi-Jon's Magnesium Citrate oral solution laxative is recalled nationwide due to microbial contamination. Approximately 8,682 bottles are affected.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1502-2022·2022-09-21

    FDA Recalls CITROMA Magnesium Citrate for Microbial Contamination

    Vi-Jon, LLC is recalling CITROMA magnesium citrate oral laxative solution due to microbial contamination. The affected product was distributed nationwide in the USA, Canada, and Panama.

    Product
    CITROMA — CITROMA (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1510-2022·2022-09-21

    Walgreens Magnesium Citrate Laxative Recalled for Microbial Contamination

    Walgreens Dye-Free Magnesium Citrate Saline Laxative is recalled nationwide due to microbial contamination affecting certain lots. Consumers should stop using the product immediately.

    Product
    Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Grape Flavor, 10 FL OZ (296 mL), Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015; NDC 0363-7162-38 UPC 3 11917 20159 7 (purple label).
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1733-2022·2022-09-21

    GFB Gluten Free Bites Dark Chocolate and Coconut recalled for undeclared cashews

    West Thomas Partners is recalling The GFB Gluten Free Bites Dark Chocolate and Coconut (UPC 856818008895) because the product contains undeclared cashews. Consumers with cashew allergies should not consume this product.

    Product
    The GFB Gluten Free Bites Dark Chocolate and Coconut 1.2oz. UPC 856818008895, 10 retail units per tray, 6 trays per wholesale case.
    Category
    Food
    Distribution
    25 states