Product Recalls in Massachusetts
Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,530 recalls have been distributed to Massachusetts in the last 12 months.
Showing 27821–27840 of 52,647 recalls
Recalled Item: PICC Catheter Trimmer Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWgard Blue PLUS Triple-Lumen CVC Kit with Blue FlexTip Catheter Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Recalled by...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kit for the Preparation of Technetium TC-99M Mebrofenin Recalled by...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for adhesive transfer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING Recalled by Smith &...
The Issue: A single lot of GENESIS II FEMORAL FIVE DEGREE VALGUS BUSHING due to a laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...
The Issue: There is a supplier quality issue with the terminal blocks which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x20cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 20x20cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 4x8cm Recalled by AROA Biosurgery, LTD. Due to...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 20x20cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 20x20cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 16x20cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.