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 8621–8640 of 29,093 recalls
Recalled Item: The Sight OLO device is a computer vision based platform Recalled by SIGHT...
The Issue: In instances where custom ranges were configured on the device post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA and DISCOVERY ULTRA Instruments Recalled by Ventana Medical...
The Issue: Potential for Fluid Leak inside a staining system that could cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000...
The Issue: Due to a component in the hemodialysis console there is the possibility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5 Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T PLUS ATRAUMATIC ADULT LP TRAY Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE DRUG FREE TRAY 22G Recalled by Bard Peripheral Vascular Inc...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 18G X 3.5 Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G Recalled by Bard Peripheral...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray Recalled by Bard...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...
The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SyncVision Systems Recalled by Volcano Corporation Due to If FFR...
The Issue: If FFR measurement(s) are made prior to an iFR/FFR co-registration/pullback...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Siemens Medical Solutions USA, Inc....
The Issue: The clip store function in the ultrasound imaging system does not work when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINQ II Insertable Cardiac Monitor Recalled by Medtronic Inc., Cardiac...
The Issue: Devices may lose functionality due to susceptibility to moisture ingress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions...
The Issue: individual components have been labelled with incorrect colours. The red and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Collagen Plugs Recalled by Lacrimedics Inc Due to The sterile pouch seal may...
The Issue: The sterile pouch seal may contain channels that could affect the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.