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. 2,691 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 23781–23800 of 29,947 recalls
Recalled Item: Pluer-evac Sahara Chest Drainage System Recalled by Teleflex Medical Due to...
The Issue: Package contains incorrect sized unit: The adult sized S-1100-08LF product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct...
The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has recently...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage:...
The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC units Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC unit because of an error code. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network Recalled by Mindray DS USA, Inc. dba...
The Issue: Software anomaly in the Panorama System software version 8.9 that manifests...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 4.75 TI Spinal System Recalled by Biomet Spine, LLC Due to...
The Issue: Multiaxial screws may not meet internal requirements related to fatigue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000V Interventional Angiography System. CAT-880B catheterization...
The Issue: The table base rotational brake that holds the table top may not always be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO Recalled by Philips...
The Issue: The firm was notified by a customer that the collimator exchange carriage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talon Grasping Device Recalled by US Endoscopy Group Inc Due to A wire...
The Issue: A wire component on the distal grasping assembly of the device became detached..
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRAL WAND W/TUBING Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) MOTOR MODULE Recalled by Microtek Medical Inc Due to This...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.