Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,858 recalls have been distributed to Maryland in the last 12 months.
Showing 8881–8900 of 29,093 recalls
Recalled Item: O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing...
The Issue: Due to product label/labeling being altered from it's approved state.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIVO Blood Collection Device 20G Recalled by Velano Vascular Due to...
The Issue: Incomplete sealing of blood collection device unit packages may produce a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iontoPATCH On-the-Go Patch Therapy Recalled by Tapemark Company Due to The...
The Issue: The dosage information on the pouch is incorrect; the primary carton label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON Systems Cholesterol (CHOL) Reagent Recalled by Beckman Coulter Inc....
The Issue: Cholesterol Reagent may fail with Out of Calibration Range Low (OCR Low)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPID 20 E Recalled by Biomerieux Inc Due to There is an error in the new...
The Issue: There is an error in the new version of the package insert. The Reading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torosa Saline-Filled Testicular Prosthesis (Size Small) Recalled by...
The Issue: Product is mislabeled for size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miami J Select Collar Recalled by Ossur Americas Due to Instructions for use...
The Issue: Instructions for use were updated to include additional information to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075)...
The Issue: The firm identified sixteen (16) faulty cartridges in LOT 210209, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ROTAPRO Recalled by Boston Scientific Corporation Due to...
The Issue: Manufacturing instructions did not include the directions to not retest the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...
The Issue: The firm identified that the Vscan Extend device will not power on because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...
The Issue: The firm identified that the Vscan Extend device will not power on because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...
The Issue: The firm identified that the Vscan Extend device will not power on because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...
The Issue: The firm identified that the Vscan Extend device will not power on because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...
The Issue: The firm identified that the Vscan Extend device will not power on because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...
The Issue: The firm identified that the Vscan Extend device will not power on because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...
The Issue: The firm identified that the Vscan Extend device will not power on because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger...
The Issue: The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...
The Issue: Manufacturing assembly error where a capacitor within the ventilator was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...
The Issue: Manufacturing assembly error where a capacitor within the ventilator was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...
The Issue: Manufacturing assembly error where a capacitor within the ventilator was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.