Virginia recalls
1025 federal recalls on file affecting Virginia - 81 Virginia-specific plus 944 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using affected Philips ALLURA X-ray tables
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using affected Philips ALLURA X-ray systems
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using affected Philips X-ray foot switches
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips ALLURA Xper system serial number
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using Philips ALLURA Xper FD10 foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips ALLURA X-ray foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideContact Philips about Allura Xper FD10C foot switch issue
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DeviceBD KiestraClass IICheck BD Kiestra ReadA system connectivity
In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this occurred, there was potential for delays in plate retrieval from the incubator while connectivity was restored. This issue was intermittent and did not affect test results, performance of the assay, or sample integrity.
- 2026-04-08FDA-DeviceSiemensClass IINationwideCheck Siemens Atellica CH A1c_E test results
A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate analyzers are not impacted by the recall. The frequency and magnitude of the negative bias and imprecision increase over time and are not consistent with the assay Instructions For Use (IFU). When this issue is present, Quality Control (QC) results demonstrate a negative trend and increased imprecision. The clinical impact of a negative (A1c_E) bias may lead to a delay in diagnosis for diabetes or lead to less-than-optimal treatment for existing diabetes.
- 2026-04-08FDA-DeviceReCor MedicalClass IINationwideDo not use ReCor Medical Paradise catheter
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
- 2026-04-08FDA-DeviceReCor MedicalClass IINationwideCheck Paradise renal denervation catheter lot M4907
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
- 2026-04-08FDA-DevicePhilipsClass INationwideCheck your Philips Respironics ventilator settings
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- 2026-04-08FDA-DevicePhilipsClass INationwideCheck your Philips Respironics ventilator settings
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- 2026-04-08FDA-DevicePhilipsClass INationwideCheck your Philips Respironics ventilator settings
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- 2026-04-08FDA-DevicePhilipsClass INationwideCheck your Philips Respironics Trilogy Evo ventilator
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- 2026-04-08FDA-DeviceAbiomedClass INationwideCheck your Impella Controller serial number
Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5 (0550-0008*) pumps.
- 2026-04-08FDA-DeviceAbiomedClass INationwideCheck your Abiomed Impella pump cassette
Increased risk of purge leaks with Generation 1 purge cassettes.
- 2026-04-08FDA-FoodHey TeaClass IIStop using HEYTEA coconut drink
Product contains undeclared milk.
- 2026-04-08FDA-FoodSuper World TradingClass IIIStop eating Mei Heong Yuen roasted peanuts
Products contain cyclamates (banned sweetener)
- 2026-04-08FDA-FoodSuper World TradingClass IIIDon't eat Mei Heong Yuen roasted peanuts
Products contain cyclamates (banned sweetener)
- 2026-04-08FDA-FoodSuper World TradingClass IIIDon't eat Mei Heong Yuen roasted peanuts
Products contain cyclamates (banned sweetener)
- 2026-04-08FDA-FoodLone Star Dairy ProductsClass INationwideStop using Lone Star Dairy milk powder
Salmonella spp. identified in finished product testing
- 2026-04-08FDA-FoodTG FoodsClass IIStop using Divided Sunset collagen peptides
The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH parenthetically or via a Contains statement.
- 2026-04-08FDA-FoodPocasClass IIIDon't drink Pocas popping boba RTD tea
Packaging integrity issue that may compromise product quality .
- 2026-04-08FDA-FoodPocasClass IIIDon't consume Pocas popping boba tea
Packaging integrity issue that may compromise product quality .
- 2026-04-08FDA-FoodPocasClass IIIDon't drink Pocas popping boba tea
Packaging integrity issue that may compromise product quality .
- 2026-04-08FDA-FoodPocasClass IIIStop using Pocas popping boba tea
Packaging integrity issue that may compromise product quality .
- 2026-04-08FDA-DrugAmneal PharmaceuticalsClass INationwideStop using Amneal Magnesium Sulfate IV bags
Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.
- 2026-04-08FDA-DrugAppco PharmaClass IINationwideStop using recalled prazosin hydrochloride capsules
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
- 2026-04-08FDA-DrugAppco PharmaClass IINationwideStop using Appco Pharma prazosin capsules
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
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