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 27421–27440 of 29,093 recalls
Recalled Item: Philips BuckyDiagnost Radiographic Recalled by Philips Healthcare Inc. Due...
The Issue: An inspection shows several IATDs (Installation Acceptance Test could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phillips Easy Diagnost Eleva DRF. Model Number: 706034 Product Usage:...
The Issue: The mirror icon on the bottom of each image could be misinterpreted as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BuckyDiagnost Radiographic. Catalog Numbers: 704031 Recalled by...
The Issue: An inspection of IATD (Installation Acceptance Test Document)IA SID (Source...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs BleaseSirius Anesthesia Workstation Recalled by Del Mar Reynolds...
The Issue: A defect in CAS I/II Absorbers in the Spacelabs Anesthesia Workstations and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 11C Plus KIT Catalog Number: Recalled...
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM KIT Catalog Number: 283913000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 7CC KIT Catalog Number: 283907000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Catalog Number:283905000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iconos R200 C20 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens has become aware of a potential malfunction and possible hazard to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG Sterile Polar Pads Recalled by Breg Inc Due to The recall was initiated...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare SureSigns VS2+ Model 863278 SureSigns VS2+ NBP and...
The Issue: VS2+ screen may lock up and stop monitoring during patient use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Senographe Essential System. The Senographe 2000D system...
The Issue: GE Healthcare has recently become aware of a potential issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell...
The Issue: Out of an abundance of caution, Ansell is implementing a voluntary recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P10 Tobii battery box (product number 510410) Product Usage - Recalled by...
The Issue: Tobii ATI customers P10 external battery pack, which contains sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atricure Inc. Recalled by Atricure Inc Due to Products from lot no. 41865...
The Issue: Products from lot no. 41865 may have been sent out with Incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG Cold Therapy Combination Units containing Sterile Polar Pads. 02356 Rev...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Body Recalled by Synthes USA HQ, Inc. Due to...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.