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. 2,800 recalls have been distributed to Maryland in the last 12 months.
Showing 15301–15320 of 29,093 recalls
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer: In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime. In vitro diagnostic testing of clinical...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation...
The Issue: An incorrect display of the Biopsy Depth Gauge graphical representation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCEA Kit ASV Yellow Stripe Microbore Recalled by Becton Dickinson & Company...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TB Series Bipolar Pacing Leads Recalled by Oscor, Inc. Due to During the use...
The Issue: During the use of some TB - Temporary Bipolar Pacing Leads, featuring the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCEA ASV Yellow Microbore Recalled by Becton Dickinson & Company Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack...
The Issue: Visual particulates within a battery Tyvek pouch. The battery is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Incubator Carestation. Neonatal incubator. Device sold under the...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda Freestanding Warmer. Device sold under the following product names:...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Warmer. Device sold under the following product names: Giraffe...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda iRes Infant Radiant Warmer. Device sold under the following Recalled...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.