Product Recalls in Pennsylvania
Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,013 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 20341–20360 of 55,602 recalls
Recalled Item: Wegmans Tuna & Provolone Packaged Sub Recalled by Wegmans Food Markets, Inc....
The Issue: Product may contain pieces of metal.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wegmans Packaged Tuna & Provolone Wheat Wrap Recalled by Wegmans Food...
The Issue: Product may contain pieces of metal.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIRECT SUPPLY Attendant VITAL SIGNS MONITOR Recalled by Mediana Co., Ltd....
The Issue: Failures were found in the temperature measurement function while in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CentraLink Data Management System software version 16.0.2 Siemens...
The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer...
The Issue: Flexible tubing connected to the liquid waste bottle can crack during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Atellica Data Manager software version 1.0 Siemens Material Number...
The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens IMMULITE 2000 XPi Immunoassay System - In vitro Chemistry Recalled...
The Issue: Flexible tubing connected to the liquid waste bottle can crack during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gabapentin Tablets USP Recalled by InvaGen Pharmaceuticals, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; failure of Impurity A test at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DRW-0739-02: Gen 2 Posterior Chairside Splint LRUL (lower right-upper left)...
The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right)...
The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right)...
The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Recalled by...
The Issue: Kit contained an incorrect catheter-tip syringe not compatible with the luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 3.2MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.