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. 2,583 recalls have been distributed to Maryland in the last 12 months.
Showing 49441–49460 of 52,535 recalls
Recalled Item: The Alere Cholestech LDX¿ high sensitivity C-Reactive Protein (hsCRP) Test...
The Issue: The Alere Cholestech LDX¿ hsCRP cassette (PN 12-807) may have increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN (TM) L-P SCREW Recalled by Smith & Nephew Inc Due to One batch of 4.5...
The Issue: One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Pro meters (catalog number 05530199160)bar code scanner. Used...
The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner....
The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX ALT AST Test Cassette Recalled by Alere San Diego, Inc....
The Issue: The recall was initiated because Alere San Diego has an update for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has received reports of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has identified potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIMGUARD Container Filters Recalled by Kimberly-Clark Corporation Due to...
The Issue: Some individual container filter units might contain thin areas that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Inline Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntellVue Info Center iX 866023 Recalled by Philips Healthcare Inc....
The Issue: If a customer creates customized trend scales in the trend review tile and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20-Pole Eco Cable Recalled by Biosense Webster, Inc. Due to Biosense is...
The Issue: Biosense is recalling the 20-Pole Eco Cable because it was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol) Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v Recalled by CareFusion 213,...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol Recalled by CareFusion...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.