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. 2,679 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 27521–27540 of 29,947 recalls
Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device...
The Issue: Power Superstand Standing Wheel chair, flex shaft (the flexible wand which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA Analyzer Pipette Tips used on Tosoh AIA-2000 Recalled by Tosoh Smd Inc...
The Issue: Visual inspection of the pipette tips indicated that some of the tips were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Four Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp....
The Issue: A firm's internal investigation led to the discovery of pinholes in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 Recalled by...
The Issue: Customers could potentially experience intermittent, unintended and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Four Lead TUR irrigation Set Recalled by Baxter Healthcare Corp. Due to A...
The Issue: A firm's internal investigation led to the discovery of pinholes in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comfort brand Ear-Loop Face Mask Recalled by Maytex Corp Due to Recent Lab...
The Issue: Recent Lab testing conducted in March 2013 indicates that the product does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superior Approach Resection Guide Assembly. Indicated for primary Recalled...
The Issue: Biomet has initiated this action following an investigation which identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp. Due...
The Issue: A firm's internal investigation led to the discovery of pinholes in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pocH-100i Recalled by Sysmex America Inc Due to The data printed on the...
The Issue: The data printed on the thermal printer may omit a digit or decimal point in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22...
The Issue: Edwards is recalling the QuickDraw Venous Cannula due to complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta Vaporizer An anesthetic vaporizer is a device used to Recalled by...
The Issue: It has come to Penlon Ltd's attention of an instance where the installation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur iPTH Calibrator 2 pk Recalled by Siemens Healthcare...
The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...
The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canister: CO2 canister with GE part numbers 1407-3200-000 Recalled by GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optovue iVue with Normative Database (NDB) with Software Version 3.0...
The Issue: Colors from the NDB comparison for Ganglion Cell Complex thickness in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.