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. 1,086 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 15321–15340 of 29,947 recalls
Recalled Item: NexGen¿ Complete Knee Solution Femoral Augment Block Distal only Recalled by...
The Issue: Screw is missing from the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm) Recalled...
The Issue: This voluntary recall is being conducted due to incorrect packaging. In one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Recalled by Horiba Instruments Incorporated Due to...
The Issue: Potential for chemical analyzer to report abnormal results due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: This recall has been initiated due to a possible leakage of a hose in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.) Recalled by The...
The Issue: A stray strand of stainless-steel cable may protrude from the heat shrink...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Instrument Arm Drape. QTY 1 Pouch Recalled by Intuitive...
The Issue: The instrument drape may tear while draping the Patient Side Cart presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 20mm Compress Device Short Anchor Plug With Drill Set Recalled by...
The Issue: Potential metal burrs in the holes of the device preventing the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Humeral Guide Wire - Ball Tip Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Bullet Tip...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice...
The Issue: Software defect: For Helical scan with ClearView function, when small arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Smooth Guide Wire - Bullet Tip Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.