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. 2,782 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,782 in last 12 months

Showing 1704117060 of 29,093 recalls

Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Cardiac Troponin I (CTNI) Flex¿ reagent cartridge Recalled...

The Issue: Concentrations for the level of biotin that does not interfere is not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 TG Recalled by Siemens Healthcare Diagnostics,...

The Issue: Concentrations for the level of biotin that does not interfere is not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2017· Bard Access Systems Inc.

Recalled Item: PowerPICC Provena Catheters Recalled by Bard Access Systems Inc. Due to...

The Issue: Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2017· Mako Surgical Corporation

Recalled Item: Makoplasty RIO Standard System Recalled by Mako Surgical Corporation Due to...

The Issue: Communication-connection error.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2017· Ormco/Sybronendo

Recalled Item: Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers...

The Issue: Buchanan Heat Pluggers will possibly overheat while used with the Elements...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2017· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet...

The Issue: Reports of product loosening or coming unscrewed from the handle.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2017· DePuy Orthopaedics, Inc.

Recalled Item: (1) Sigma HP Cemented Trochlea Size 1 Narrow Left Recalled by DePuy...

The Issue: The SIGMA¿ HP PFJ Cemented Trochlear Implants, a standalone component of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2017· W & H DentalWerk Burmoos GMBH - Site 1

Recalled Item: Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot Recalled by...

The Issue: During continuous postmarket surveillance activities, we have noticed a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STRL Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X11X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Merit Medical Systems, Inc.

Recalled Item: Flex-Neck Classic Peritoneal Dialysis Catheter (Pediatric) Product Usage: If...

The Issue: Mix-up between adult and pediatrics PD catheter.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 125 DEG X Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER L H TROC NAIL 320X9X125 Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Nidek Inc.

Recalled Item: AUTO REF/KERATOMETER ARK-1s Recalled by Nidek Inc. Due to There is possibly...

The Issue: There is possibly a difference between the measured dioptric value of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 11X180 125DG STRL Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC END CAP STER TROC Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Ad-Tech Medical Instrument Corporation

Recalled Item: Disposable Drill Kit which includes two drill bits Recalled by Ad-Tech...

The Issue: There is a possibility that DDK2-2.4-30X Disposable Drill Kits, Lot Number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing