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. 2,735 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 18581–18600 of 29,947 recalls
Recalled Item: ArrowADVANTAGE5" Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Recalled by Arrow...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLUE BURN SHEET Recalled by Dukal Corp. Due to Intact carton revealed...
The Issue: Intact carton revealed presence of shredded burn sheets
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans SFILL 360 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 1000 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 100 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASER Amplifier Recalled by Solta Medical Inc Due to Potential inaccurate...
The Issue: Potential inaccurate calibration by service depot repair, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 2000 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Product Usage: The da Vinci Recalled by...
The Issue: da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftLab Software Laboratory information system to be used in a Recalled by...
The Issue: Display of lab results based on incorrect LOINC code/test descriptions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Precision Glide Needle 18G x 1 RB Recalled by Becton Dickinson & Company...
The Issue: Hub damage resulting in breakage and/or leakage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...
The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...
The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...
The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01 Recalled by...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: Carestream found a single unit where four screws in the assembly were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium iCAST Balloon Expandable Covered Stent Recalled by Atrium Medical...
The Issue: Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.