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. 2,674 recalls have been distributed to Maryland in the last 12 months.
Showing 27141–27160 of 29,093 recalls
Recalled Item: Oxford Uni Knee System Recalled by Biomet U.K., Ltd. Due to Investigation of...
The Issue: Investigation of complaints found excessive use of the instrument could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...
The Issue: A defect on the master-side connector block of the pneumatic tool changer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HD Still Capture System ConMed Linvatec . Captures Recalled by Linvatec...
The Issue: The VP1600 HD Still Capture Image System is recalled due to an anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...
The Issue: The recall was initiated because Shimadzu Corporation has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy....
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSS Select medical products***Biopsy Punches*** Disposable manual instrument...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....
The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...
The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.