Recalls distributed in Pennsylvania
These notices name Pennsylvania in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
5,886 stored notices name Pennsylvania, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.
Reported May 27, 2026
Stoltzfus Family Farm Sour Cream and Onion cheese curds, 8-ounce
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stoltzfus Family Dairy LLC
FDA (openFDA food enforcement)
Reported May 20, 2026
Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I
High riskUsing this product could cause serious injury, illness or death — stop using it now.Arrow International, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dexcom, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 20, 2026
Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Omnicell, Inc.
FDA (openFDA device enforcement)
Reported May 20, 2026
QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported May 20, 2026
Swad Orange Flavored Masala Candy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raja Foods and Vegetables Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 20, 2026
Diowave Laser System, REF: Diowave 250W
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Technological Medical Advancements LLC
FDA (openFDA device enforcement)
Reported May 13, 2026
One Step 10A in vitro diagnostic test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DFI Co., Ltd.
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe Medical, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece…
High riskUsing this product could cause serious injury, illness or death — stop using it now.French Broad Chocolate Factory
FDA (openFDA food enforcement)
Reported May 13, 2026
Costco Service Deli Department 63 MEATLOAF SEASONING MORE FLV Pack Size: 4-5lb. Bags Net Weight: 20lbs Allergy…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Griffith Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 13, 2026
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2026
Garland Fresh Peeled Garlic 6 oz. bag
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tops Markets LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 13, 2026
LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wehah Farms
FDA (openFDA food enforcement)
Reported May 6, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported May 6, 2026
iLet Bionic Pancreas, REF: BB1001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beta Bionics, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Leksell Vantage Arc System REF: 1053958
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Negita Cracker- Shrimp 2.8oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hadson (Toko) Trading Co. Inc.
FDA (openFDA food enforcement)
Reported May 6, 2026
Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator, 6mm-7mm-8mm, REF 1204-08
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diversatek Healthcare
3 more products in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.