Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,067 recalls have been distributed to Virginia in the last 12 months.
Showing 16141–16160 of 29,425 recalls
Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 (Stitching Patient Support) 709030 Recalled by Philips...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Single Detector (Stitching Patient Support) 712020 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 (Stitching Patient Support) 712225 Recalled by Philips...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips Medical Systems Gmbh, DMC Due to...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based...
The Issue: The margin tool in Leksell GammaPlan 11.1 systematically overestimates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BuckyDiagnost Ceiling System (Stitching Patient Support) 704031 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Gantry rotation or...
The Issue: Gantry rotation or proton irradiation can be allowed even if apertures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: Recalled by...
The Issue: Genicon is providing updated IFU labeling to users to provide clarity on how...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood parameter monitoring system 500 H/SAT Recalled by Terumo...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitor with one Blood Parameter Module and one HSat Probe Recalled by...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT CLEARVUE isp Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Certain NAUTILUS DELTA Port Kit product code / lot number combinations may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This is an accessory to Intelect Advanced Recalled by DJO, LLC Due to The...
The Issue: The device accessories were not labeled with appropriate latex warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...
The Issue: Potential hardware issue which may cause thermal effects and possible damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...
The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.