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. 2,597 recalls have been distributed to Maryland in the last 12 months.
Showing 41441–41460 of 52,535 recalls
Recalled Item: Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct...
The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC units Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC unit because of an error code. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network Recalled by Mindray DS USA, Inc. dba...
The Issue: Software anomaly in the Panorama System software version 8.9 that manifests...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has recently...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage:...
The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BADIA Ground Cumin Recalled by Badia Spices, Inc. Due to Undeclared Peanut
The Issue: Undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cinnamon Almonds Recalled by Trader Joes Company Due to Undeclared Peanuts
The Issue: Trader Joes Company is recalling its 16 ounce packages of Trader Joes...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Captopril Tablets Recalled by Wockhardt Usa Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: out of specification for thickness.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polaris 4.75 TI Spinal System Recalled by Biomet Spine, LLC Due to...
The Issue: Multiaxial screws may not meet internal requirements related to fatigue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LACTATED RINGER'S IRRIGATION Recalled by Hospira Inc. Due to Non-Sterility:...
The Issue: Non-Sterility: Confirmed customer report of dark, fibrous particulates...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO Recalled by Philips...
The Issue: The firm was notified by a customer that the collimator exchange carriage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000V Interventional Angiography System. CAT-880B catheterization...
The Issue: The table base rotational brake that holds the table top may not always be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giant Eagle Irish Soda Bread Recalled by Giant Eagle, Inc. Due to Undeclared...
The Issue: Giant Eagle has announced a voluntary recall of Irish Soda Bread due to an...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER RESISTANT WAND - STERILE Recalled by Microtek Medical Inc Due to This...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRAL WAND W/TUBING Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.