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.

52,535 total recalls
2,674 in last 12 months

Showing 2890128920 of 29,093 recalls

Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2011· The Anspach Effort, Inc.

Recalled Item: Anspach Twist Drill for 1.5mm x 4mm screw. Recalled by The Anspach Effort,...

The Issue: Cutter was longer than was stated on the label

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2011· The Anspach Effort, Inc.

Recalled Item: AnspacSingle use Sterile bone cutting burs.h Twist Drill Recalled by The...

The Issue: Cutter was longer than was stated on the label

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2011· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When performing a...

The Issue: When performing a secondary capture generated from GSI Viewer, the header...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2011· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...

The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...

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

Class III — Low RiskOngoing
Medical DeviceMarch 24, 2011· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...

The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...

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

Class III — Low RiskOngoing
Medical DeviceMarch 24, 2011· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...

The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...

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

Class III — Low RiskOngoing
Medical DeviceMarch 21, 2011· Stryker Spine

Recalled Item: Stryker Reliance AL Implant Blocker (Various sizes) The SLIDE Implant...

The Issue: Stryker Spine has received six reports regarding the breakage of one or more...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2011· Hospira Inc.

Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to May go to a white...

The Issue: May go to a white screen due to a problem with the SOM2 module. A white...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2011· Hospira Inc.

Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to May go to a white...

The Issue: May go to a white screen due to a problem with the SOM2 module. A white...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2011· Biomet Spine LLC.

Recalled Item: LANX Recalled by Biomet Spine LLC. Due to Biomet Spine, LLC. announces...

The Issue: Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2011· Ge Healthcare It

Recalled Item: Imagecast PACS is an image management system intended to be Recalled by Ge...

The Issue: In Imagecast PACS versions prior to 3.6.51.01, the estimated magnification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2011· The Anspach Effort, Inc.

Recalled Item: ****** 3mm Diamond Ball. Used for cutting and shaping bone. Recalled by The...

The Issue: Due to three batches of product may have diamond grit size larger than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2011· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-Ray System Recalled by Philips Medical...

The Issue: Multiple software defects which could impact the performance or reliability...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardioplegia Delivery Set- Catalog Number:165720 and Catalog...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardioplegia Delivery Sets Catalog Code: 204880 Product Usage:...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular and Perfusion Procedure Kits Catalog Codes:...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Cardioplegia Delivery Set- Item Number: 16130 Product Usage: The...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing