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. 1,184 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 1581–1600 of 55,602 recalls
Recalled Item: NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClariTEE Miniaturized TEE probe. Model Number: CLT-010. Ultrasound...
The Issue: Production assembly error resulting in the potential for reversed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK System Non_DEHP Extenstion Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 88-Series Washer- Disinfector. Model Number: 88-5. Recalled by...
The Issue: Potential for device to overheat during operation if the circulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX...
The Issue: To provide further information to the user to ensure proper use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bevacizumab (Avastin) Injection Recalled by Fagron Compounding Services Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuoDERM" Extra Thin dressings are highly flexible Recalled by ConvaTec, Inc...
The Issue: Wound dressing may have foreign matter on the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sharesource Connectivity Platform for Use with Homechoice Claria Product...
The Issue: Vantive has identified a software defect within the Sharesource Claria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Verio Dot Upgrade. Model Number: 10684334. Recalled by Siemens...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Connectom.X. Model Number: 11371480. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Cima.X (DE). Model Number: 11647158. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Verio Dot. Model Number: 10684333. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mMR. Model Number: 10433372. Recalled by Siemens Medical Solutions...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra fit. Model Number: 10849580. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396 Recalled by...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Vida Fit. Model Number: 11410481. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number:...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.