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. 2,685 recalls have been distributed to Maryland in the last 12 months.
Showing 26181–26200 of 29,093 recalls
Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...
The Issue: It was discovered that Carestream received a report from a customer that 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use. PN...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...
The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek FMS Intermediary Tubing with One-Way valve Product Code:...
The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649...
The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2244.3808 Recalled by Camlog Usa Due to Product not cleared for sale/use in...
The Issue: Product not cleared for sale/use in the United States.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2244.3820 Recalled by Camlog Usa Due to Product not cleared for sale/use in...
The Issue: Product not cleared for sale/use in the United States.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...
The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-LIFT Extension Shims Extension shims are manufactured from grade 5...
The Issue: Fit variation among all lots of S-LIFT extension shims with corresponding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys...
The Issue: Based on a review of historic packaging validations, it was determined that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical MicroFuse Putty Recalled by Globus Medical, Inc. Due to The...
The Issue: The sterility of this product to a Sterility Assurance Level (SAL) of 10(-6)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2244.4308 CONELOG Titanium Base CC ¿4.3GH2 0.8 inkl HS Product Recalled by...
The Issue: Product not cleared for sale/use in the United States.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.