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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 48,122 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.

Medical devices

Reported Apr 1, 2020

Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.

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

Medline Industries Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

RayStation standalone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 7.0, 8.0, 8.1,…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part…

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

Skytron, Div. The KMW Group, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

Columbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K NN070K NN071K NN072K…

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

Aesculap Implant Systems LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and…

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

CME America, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2020

Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl. oz. (435 mL) UPC: 041548610047 Case UPC: 10041548610044

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

Dreyers Grand Ice Cream, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Drugs

Reported Mar 25, 2020

Lisinopril/HCTZ 20mg/12.5mg Tablet, QTY: 30 tablets per blister card, MFG: Lupin Pharma Baltimore, MD 21202, NDC…

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

RemedyRepack Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Mar 25, 2020

IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

LEGION PS High Flex XLPE size 5-6 9mm Articular Insert

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2020

Vita Wild Herring in Wine Sauce 32oz plastic jar, UPC 22635 40011, 6 jars per case Ready to Eat Keep Refrigerated

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

Vita Food Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2020

OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe; STERILE R, Product Code: 359100, Dimensions:…

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

Xtant Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general…

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

Cardinal Health 200, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

BodyGuard Microset REF A120-003XYVA, Sterile EO, Tubing: 150 in. (380 cm), Prime Vol: approx. 8ml Product Usage: The…

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

CME America, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

GREAT VALUE¿ Pure Granulated Sugar, 10 lbs. Sold as individual bags on a unitized 1/2 pallet 78 bags to a 1/2 pallet.

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

Domino Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

Butterfly Shrimp 16/20, 50 lb. cases

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

Les Chateaux De France

FDA (openFDA food enforcement)

Food

Reported Mar 18, 2020

Pure Cane Granulated Sugar, Single 10 lb. package, 156 paper bags on 2 1/2 CHEP pallets

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

Maryland Packaging, Ltd.

FDA (openFDA food enforcement)

Food

Reported Mar 18, 2020

Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato…

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical…

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

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Bard Biopsy EnCor Probe, Stereotactic/Ultrasound 7G, REF number ECP017G, packaged individually in sterile pouches, 5…

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

Bard Peripheral Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733

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

Beckman Coulter Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible pouch

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

Blendtopia Products, LLC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2020

CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)

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

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

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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.