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. 2,871 recalls have been distributed to Maryland in the last 12 months.
Showing 6001–6020 of 29,093 recalls
Recalled Item: ellacor System with Micro-Coring Technology-Indicated for use by medical...
The Issue: Potential failure of a bearing adhesive joint that can occur due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes and Surgical Room Turnover (SRT) Kits: Recalled...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINEAR 7.5Fr.IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION 7 Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YAMATO PLUS IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS 7.5Fr IAB Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANS-RAY IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGA 7.5Fr.IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REINFORCED INTRODUCER SET Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGA 8Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS 8Fr. IAB Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000C XGCP-930AA TABLE SIDE CONSOLE Recalled by Canon Medical System,...
The Issue: The C-arm, used to set the position and angle of the x-ray exposure field,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use...
The Issue: The STATCLAVE G4 is a dynamic air removal (prevacuum) tabletop steam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gore Tips Set Device Recalled by Creganna Medical Devices Due to Three lots...
The Issue: Three lots of product may be labeled with an incorrect expiration day
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use...
The Issue: The STATCLAVE G4 is a dynamic air removal (prevacuum) tabletop steam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Urine Control Level 2- intended for in vitro diagnostic use...
The Issue: (1) There is vial to vial variation resulting in some vials recovering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HoverMatt Recalled by Stryker Sustainability Solutions Due to 39-inche-wide...
The Issue: 39-inche-wide inflatable air transfer mattress packages contain 34-Inch-wide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ringed DxI Reaction Vessels (RVs) Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter, Inc. is recalling Ringed DxI Reaction Vessels (RVs) as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno-Angiography systems developed for single and biplane diagnostic...
The Issue: Due to a hardware issue in the cable connectors of the system generator, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.