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. 1,983 recalls have been distributed to Virginia in the last 12 months.
Showing 17341–17360 of 29,425 recalls
Recalled Item: LPS-FLEX PRECOAT FEMORAL B-R LPS-FLEX PRECOAT FEMORAL C-L LPS-FLEX PRECOAT...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 8 INCH BEADED FC 12X200MM STR STD BODY/NECK 13X200MM Recalled by...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...
The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...
The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...
The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: Recalled by...
The Issue: Component of the Lap-Band system was missing from the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...
The Issue: It was discovered that the product units it imported may, at peak levels,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...
The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility with Integrity R3.2 Recalled by Elekta Limited Due to Potential for...
The Issue: Potential for positional errors following automatic table movement (ATM).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity R1.2 Recalled by Elekta Limited Due to Potential for positional...
The Issue: Potential for positional errors following automatic table movement (ATM).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to When calculating...
The Issue: When calculating electron Monte Carlo dose with a very large number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio...
The Issue: While in Full Disclosure playback, a user may inadvertently close the Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia Prime software Recalled by Phadia Ab Due to We want to inform all...
The Issue: We want to inform all Phadia 250 system operators performing EliA Assays not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDAN Telemetry Transmitter Recalled by Edan Diagnostics Due to Firm became...
The Issue: Firm became aware that it distributed 7 units in the U.S. that included a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to The syringe...
The Issue: The syringe plunger grippers may fail to automatically close around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Pump Recalled by CareFusion 303, Inc. Due to The syringe plunger...
The Issue: The syringe plunger grippers may fail to automatically close around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectra System/Legacy Guided Surgery Handle Kit (Part Number: G-HK) Spectra...
The Issue: The Spectra System/Legacy Guided Surgery Handle Kit had guided handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated...
The Issue: Potential for cracked luer hubs
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.