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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.

5,819 stored notices name Pennsylvania, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.

Medical devices

Reported Jul 9, 2025

HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hardy Diagnostics

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2025

Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Peak Cocktails

FDA (openFDA food enforcement)

Medical devices

Reported Jul 2, 2025

REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

DxI 9000 Access Immunoassay Analyzer C11137

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson Infusion Therapy Systems, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 Release…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bigfoot Biomedical

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 2, 2025

Carley s Soft Baked Iced Lemon Cookies, 5.34oz Plastic Tray, clear film overwrap w/ Label, 12 units per case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carley's Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 2, 2025

FIREHOOK ARTISAN BAKED CRACKERS CLASSIC SEA SALT NET WT. 8 OZ (227g) INGREDIENTS: ORGANIC WHEAT FLOUR, ORGANIC HONEY,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Firehook

FDA (openFDA food enforcement)

Food

Reported Jul 2, 2025

Isabelle's Kitchen, Inc, Greek Pasta Salad, 4.5 lb., High density polyethylene container with sealed lid. Kings Where…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Isabelle's Kitchen, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 2, 2025

Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog Number: JP-24-6.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Jewel Precision Sheet Metal & Machining Co., Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Spectral CT. Computed tomography X-ray system.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2025

Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Balt USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2025

ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pump

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2025

Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Preat Corp.

FDA (openFDA device enforcement)

Food

Reported Jun 25, 2025

Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., Item Code 407079, UPC 13454.38482. This…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Reser's Fine Foods, Inc. dba Fresh Creative Foods

FDA (openFDA food enforcement)

Food

Reported Jun 25, 2025

Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Yerba Prima Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 18, 2025

Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bd Switzerland Sarl

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Allon 2001. Part Number: 200-00263

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Belmont Instrument LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Contamac Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Covidien

FDA (openFDA device enforcement)

Food

Reported Jun 18, 2025

Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lipman Family Farms

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 18, 2025

KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microbiologics Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 18, 2025

3909520 2/5# IMPERIAL FRESH CUCUMBER DICED 3/8 SK-ON ALL LOT CODES 480414 2/5 # IMPERIAL FRESH FC CUCUMBER STRIPED AND…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sysco Corporation

7 more products in this recall

FDA (openFDA food 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.