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.
5,896 stored notices name Pennsylvania, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.
Reported Sep 16, 2020
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…
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)
Reported Sep 16, 2020
SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hager & Meisinger GmbH
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh US
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Arrowhead Mills Organic Yellow Popcorn, 28oz bag, UPC: 0 7433347665 8, 6 retail bags per wholesale case, case item code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hometown Food Company
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
FDA (openFDA device enforcement)
Reported Sep 16, 2020
PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroPort Orthopedics Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2020
QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Talladium Luminesse Zirconia Discs, Zirconia HT Disc 98x20mm A1, Shaded Zirconia Blend 2.0 50# A1, Model No.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Talladium Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2020
SOUTHERN GROVE; MIXED NUTS; LESS THAN 50% PEANUTS; PEANUTS, ALMONDS, CASHEWS, HAZELNUTS, & PECANS; with Sea Salt; NET…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Superior Nut Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Signature Select Chewy Granola Bars, Chocolate Chip, Family Pack, 18 bars, UPC 021130-283637. 18-0.84 oz. Net Wt 15.2…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Treehouse Foods
FDA (openFDA food enforcement)
Reported Sep 9, 2020
BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring of end tidal carbon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
The Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Sub Shop-Red Onions. Expiration 7/31/2020. Ingredients raw red onion.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Eagle
53 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 9, 2020
Newman's Own Organics, Newman's Special Decaf Medium Roast, Ground Coffee, 10 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keurig Dr Pepper, Inc.
FDA (openFDA food enforcement)
Reported Sep 9, 2020
RONZONI SINCE 1915 Smart Taste Extra Wide Noodle Style 2.5x the Fiber of Regular Pasta Net Wt. 12OZ (340g). UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Riviana Foods Inc.
FDA (openFDA food enforcement)
Reported Sep 9, 2020
Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stimwave Technologies Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster (israel), Ltd.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Klarity Vacuum Bags, Item Nos. R7504-30C, R7504-35BC,R7504-35C, R7644-32.5BC, RC7221-25BC, RC7504-17.5C - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Klarity Medical Products LLC
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 6.0mm REF NVTKIT-C6-5, Rx Only, Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neurovision Medical Products Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coated Micro-Plate-IVD…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OraSure Technologies, Inc.
1 more product 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.