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. 1,107 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 14801–14820 of 29,947 recalls
Recalled Item: Abutment Screw Retrieval Instrument 3.0/NP - Product Usage: The instruments...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Tap Tapered WP Single-Pat - Product Usage: The Guided Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Tapered WP 5x10 mm Single-Pat - Product Usage: Drills Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Tapered RP 4.3x11.5 mm Single-Pat - Product Usage: The Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Tapered NP 3.5x11.5 mm Single-Pat - Product Usage: The Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guided Start Drills/Counterbore NobRpl NP - Product Usage: The Guided...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gridlock Ankle Screw Driver Bit - Product Usage: Recalled by Trilliant...
The Issue: A screwdriver used to facilitate implant insertion and removal was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure kits include devices from the affected lots distributed OUS...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow Disposable Cartridge Recalled by Vyaire Medical Due to Testing has...
The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow Disposable Cartridge with IV Extension Set Recalled by Vyaire Medical...
The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo Grasp Auto Suture Grasper 5mm The Recalled by COVIDIEN LLC Due...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo Clinch II Auto Suture Grasper Recalled by COVIDIEN LLC Due to...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...
The Issue: 2.5 Truliant Fit Trays were mismarked as 3
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits Recalled...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity Recalled by Elekta Limited Due to Users need to be aware when...
The Issue: Users need to be aware when using these protocols for daily on line plan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Xstar Slit Knife 2.4 mm Recalled by Beaver Visitec Due to Mislabeling
The Issue: Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Recalled by...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.