Medical DeviceOct 30, 2019
Medline Industries Semi-Rigid Suction Canister, 3000cc recall — FDA Z-0174-2020
Potential for the Semi-Rigid canister lid to fragment during use.
Class IIFDA: OngoingMedline Industries Inc.
Latest records
Latest recalls — page 1141
The newest recall records with useful source details are listed here.
Medical DeviceOct 30, 2019
Community Products Rifton TRAM Low Base, SKU K320, powered lift device recall — FDA Z-0165-2020
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Class IIFDA: TerminatedCommunity Products, LLC
Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound recall — FDA Z-0183-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Medical DeviceOct 30, 2019
Siemens Medical Solutions USA Mammomat Revelation with software version VC10 and Biopsy recall — FDA Z-0160-2020
An error can occur when performing a biopsy using the InSpect function. The acquisition workstation may become unresponsive to normal user interaction, can only take place in rare cases
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceOct 30, 2019
Life Technologies Holdings Pte Torrent Suite Dx Software Version (IUO) 5.2 recall — FDA Z-0185-2020
Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx Instrument System, incorrectly displays a positive result when a different analytical or de novo variant is detected at…
Class IIFDA: TerminatedLife Technologies Holdings Pte Ltd
Medical DeviceOct 30, 2019
Brainlab AG Patient Data Manager, Model/Catalogue Numbers: 25100-09 - PATIENT DATA MANAGER recall — FDA Z-0176-2020
The Brainlab Patient Data Manager software (PDM) in combination with the Brainlab iPlan CMF/Cranial/ENT/Spine software 2.1.1, 2.2.0, 2.2.1, 2.3.0, 2.3.1, 2.4.0, 2.5.0, 2.5.1 (if used in…
Class IIFDA: TerminatedBrainlab AG
Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound recall — FDA Z-0181-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Medical DeviceOct 30, 2019
Community Products Rifton TRAM Standard Base, SKU K310, powered lift device recall — FDA Z-0164-2020
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Class IIFDA: TerminatedCommunity Products, LLC
Medical DeviceOct 30, 2019
Xintec OptiLITE, Products for Laser Surgery, Model # CGH1080F, 800 micron single-use holmium recall — FDA Z-0162-2020
It has been determined that a lot of fiber lasers were programmed incorrectly. As a result, the fibers from this lot will produce an error and will not allow the user to use the laser when…
Class IIIFDA: TerminatedXintec Corp
Medical DeviceOct 30, 2019
Smiths Medical ASD GRIPPER Needles sold individually recall — FDA Z-0189-2020
Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound recall — FDA Z-0179-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Medical DeviceOct 30, 2019
Baxter Healthcare EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following recall — FDA Z-0167-2020
Potential ability to leak once used for compounding.
Class IIFDA: TerminatedBaxter Healthcare Corporation
Medical DeviceOct 30, 2019
Deerfield Imaging IMRIS MR/X-ray head fixation device, Model HFD200 recall — FDA Z-0163-2020
Breaking of the HFD200 Drive Knob force indicator due to over-torqueing of the drive knob beyond the maximum allowable pinning force specification may result in the clinical staff…
Class IIFDA: TerminatedDeerfield Imaging, Inc.
Medical DeviceOct 30, 2019
Siemens Healthcare Diagnostics Atellica IM 1600 Analyzer, (SW) version V1.19.0 and V1.19.2 recall — FDA Z-0205-2020
Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300 Analyzer and Atellica IM 1600 Analyzer SW V 1.19.0 and 1.19.2
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceOct 30, 2019
Candela Canister HFC-134a /1000g, ALUM, 15 pack Product Number: 1600-00-0219 Revision .0C recall — FDA Z-0207-2020
The canister neck bushing may become loose and separate from the body of the canister during use. The issue occurs only when the canisters are used in Candela legacy devices that utilize…
Class IIFDA: TerminatedCandela Corporation
Medical DeviceOct 30, 2019
GN Otometrics The ICS CHARTR EP 200 recall — FDA Z-0170-2020
There is a risk to the healthcare professional or patient of exposure to undergrounded electrical surfaces which may result in an electrical shock.
Class IIFDA: TerminatedGN Otometrics
Medical DeviceOct 30, 2019
Becton Dickinson & Company BD Vacutainer Push Button Blood Collection Set with Pre-Attached recall — FDA Z-0193-2020
Separation of front and rear barrels upon activation of the safety feature that retracts the needle
Class IIFDA: TerminatedBecton Dickinson & Company
Medical DeviceOct 30, 2019
Siemens Healthcare Diagnostics Atellica IM 1300 Analyzer, (SW) version V1.19.0 and V1.19.2 recall — FDA Z-0204-2020
Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300 Analyzer and Atellica IM 1600 Analyzer SW V 1.19.0 and 1.19.2
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceOct 30, 2019
Candela Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant recall — FDA Z-0206-2020
The canister neck bushing may become loose and separate from the body of the canister during use. The issue occurs only when the canisters are used in Candela legacy devices that utilize…
Class IIFDA: TerminatedCandela Corporation
Medical DeviceOct 30, 2019
Life Technologies Holdings Pte Torrent Suite Dx Software Version 5.8 recall — FDA Z-0188-2020
Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx Instrument System, incorrectly displays a positive result when a different analytical or de novo variant is detected at…
Class IIFDA: TerminatedLife Technologies Holdings Pte Ltd
FoodOct 30, 2019
Mrs. Stratton's Salads Tuna salad under the following brand names: BALLARDS FARM recall — FDA F-0063-2020
Potential contamination from Listeria monocytogenes.
Class IFDA: TerminatedMrs. Stratton's Salads, Inc.
FoodOct 30, 2019
Lipari Foods Operating Company, LLC Premo Signature Cranberry Almond Chicken Salad croissant recall — FDA F-0089-2020
Products contain chicken which has been recalled by supplier because it may be contaminated with Listeria monocytogenes
Class IFDA: TerminatedLipari Foods Operating Company, LLC.
FoodOct 30, 2019
weaver fundraising Trails End Sweet and Savory Collection, containing White recall — FDA F-0073-2020
Inaccurate Nutrition Facts and ingredient declaration including undeclared almonds, cashews, and pecans
Class IIFDA: Terminatedweaver fundraising
FoodOct 30, 2019
Veritable Vegetable Jayleaf Fresh Baby Spinach recall — FDA F-0068-2020
Notified by customer of presumptive positive results for Enterohemorrhagic E. coli (ECHEC)/Shiga Toxin-Producing E. coli (STEC) in fresh spinach.
Class IFDA: TerminatedVeritable Vegetable
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026180 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories