All recall categories

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 Dec 21, 2022

Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer

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

ARROW INTERNATIONAL Inc.

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 21, 2022

DeRoyal MINOR ORAL / ENT PACK, REF 89-2576.15

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

DeRoyal Industries Inc.

155 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 14, 2022

0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx only NDC 0264-5802-00 B. Braun Medical Inc.…

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

B. Braun Medical, Inc.

FDA (openFDA drug enforcement)

Food

Reported Dec 14, 2022

ARASHAN brand mixed dried fruit packaged in 1lb clear plastic bags with a sticker label. UPC: 850008491368

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

Bek12 Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors…

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

Bunnell, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 14, 2022

Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case

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

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Food

Reported Dec 14, 2022

Weis Quality Premium Ice Cream Sea Salt Caramel Ripple 1.5 Quart (1.42 L) UPC 041497-01288

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

Weis Markets, Inc., Ice Cream Division

FDA (openFDA food enforcement)

Medical devices

Reported Dec 7, 2022

Accelerate PhenoTest BC kit REF 10101018

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

Accelerate Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

Alcon Custom Pak Surgical Procedure Pack

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 7, 2022

Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. individually wrapped plastic packages - 12 units per case UPC…

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

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 7, 2022

CMV IgM EIA, in vitro diagnostic.

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

Bio-Rad Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel…

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

Greer Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200…

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

GS Biomark LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

eSuction Small Cavity, Model ET2005

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

Endo-Therapeutics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

Hamilton-C6

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013

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

Kamiya Biomedical Company, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected…

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

Medical Action Industries, Inc. 306

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed Tip, 19G, Model…

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

Pajunk Medical Systems, LP

FDA (openFDA device enforcement)

Drugs

Reported Nov 23, 2022

Fyarro (sirolimus protein-bound particles for injectable suspension (albumin-bound), 100 mg per vial, NDC 80803-153-50,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Aadi Bioscience

FDA (openFDA drug enforcement)

Food

Reported Nov 23, 2022

Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case

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

Abbott Laboratories

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2022

Hill-Rom Progressa Bed System

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Pennsylvania recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Other states

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.