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. 2,636 recalls have been distributed to Maryland in the last 12 months.
Showing 38481–38500 of 52,535 recalls
Recalled Item: 2.4MM locking screw SLF-TPNG with Stardrive Recess 18 mm. Intended Recalled...
The Issue: It was discovered that the above part number and lot of 2.4mm Locking Screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RBT Recalled by BioHorizons Implant Systems Inc Due to An incorrect label...
The Issue: An incorrect label reading 10.5mm and not the specified 15mm was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDROCHLOROTHIAZIDE CAPSULES Recalled by Amerisource Health Services Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natures Promise Organic Edamame in Pod Recalled by Green Organic Vegetables...
The Issue: Product contains undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Natures Promise Organic Shelled Edamame Recalled by Green Organic...
The Issue: Product contains undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Computed Tomography X-ray system Recalled by Philips...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...
The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...
The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Defective Delivery System; potential to have inaccurate dosage delivery
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Defective Delivery System; potential to have inaccurate dosage delivery
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DA-2006P - Defibrillator / Pacer Analyzer Recalled by BC Group International...
The Issue: Device is not functioning as intended: Two wires running to the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DGDE Recalled by Implant Direct Sybron Manufacturing, LLC Due to Implant...
The Issue: Implant Direct Sybron Manufacturing, LLC is recalling 26 lots of DGDE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProTrack Microcatheter. Model/Catalog Numbers CIC38-145 Recalled by Baylis...
The Issue: Microcatheter may have circumferential defects (cracks) along its shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 5001102 MPS Delivery Set w/ arrest agent and additive cassettes...
The Issue: The products have been found to intermittently exhibit a seal failure during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rainbow Reusable Sensors. RAINBOW DCI-DC3 Recalled by Masimo Corporation Due...
The Issue: These sensors were manufactured with incompatible configurations. This could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.