FDA Device recall Z-2995-2018

Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC

FDA Device
Class II
terminated
Published 2018-09-19

On 2018-09-19 the FDA classified a Class II recall of Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC by Ohio Medical, citing the care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal may come in contact with the pump causing an electric short leading to damage to wiring and resulting in….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2995-2018
Classification	Class II
Status	terminated
Initiated	2018-08-14
Published	2018-09-19
Last updated	2026-09-13 11:54 UTC
Company	Ohio Medical
Distribution	US

Product

Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style 758000, Model CARE-E-VAC 3, Ohio Medical LLC The care-e-(R)3 is a portable medical aspirator used to suction fluids or foreign bodies from a patient. The primary intended use is to aspirate saliva, mucous, vomitus or other aspirant from the mouth or airway to allow adequate respiration or ventilation of the patient.

Reason

The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal may come in contact with the pump causing an electric short leading to damage to wiring and resulting in loss of function or an inoperable unit under battery power.

Identifiers

code_info	(a) style 758010 Serial Numbers: CDS5000 CDS5001 CDS5002 CDS5003 CDS5004 CDS5005 CDS5006 CDS5007 CDS5008 CDS… (a) style 758010 Serial Numbers: CDS5000 CDS5001 CDS5002 CDS5003 CDS5004 CDS5005 CDS5006 CDS5007 CDS5008 CDS5009 CDS5010 CDS5011 CDS5012 CDS5013 CDS5014 CDS5015 CDS5016 CDS5017 CDS5018 CDS5019 CDS5020 CDS5021 CDS5022 CDS5023 CDS5024 CDS5025 CDS5026 CDS5027 CDS5028 CDS5029 CDS5030 CDS5031 CDS5032 CDS5033 CDS5034 CDS5035 CDS5036 CDS5037 CDS5038 CDS5039 CDS5040 CDS5041 CDS5042 CDS5043 CDS5044 CEV3X0076 CEV3X0077 CEV3X0078 CEV3X0079 CEV3X0080 CEV3X0081 CEV3X0082 CEV3X0083 CEV3X0084 CEV3X0085 CEV3X0086 CEV3X0087 CEV3X0088 CEV3X0089 CEV3X0090 CEV3X0091 CEV3X0092 CEV3X0093 CEV3X0094 CEV3X0095 CEV3X0096 CEV3X0097 CEV3X0098 CEV3X0099 CEV3X0100 CEV3X0101 CEV3X0102 CEV3X0103 CEV3X0104 CEV3X0105 CEV3X0106 CEV3X0107 CEV3X0108 CEV3X0109 CEV3X0110 CEV3X0111 CEV3X0112 CEV3X0113 CEV3X0114 CEV3X0115 CEV3X0116 CEV3X0117 CEV3X0118 CEV3X0119 CEV3X0120 CEV3X0121 CEV3X0122 CEV3X0123 CEV3X0124 CEV3X0125 CEV3X0176

code_info

(a) style 758010 Serial Numbers: CDS5000 CDS5001 CDS5002 CDS5003 CDS5004 CDS5005 CDS5006 CDS5007 CDS5008 CDS…

(a) style 758010 Serial Numbers: CDS5000 CDS5001 CDS5002 CDS5003 CDS5004 CDS5005 CDS5006 CDS5007 CDS5008 CDS5009 CDS5010 CDS5011 CDS5012 CDS5013 CDS5014 CDS5015 CDS5016 CDS5017 CDS5018 CDS5019 CDS5020 CDS5021 CDS5022 CDS5023 CDS5024 CDS5025 CDS5026 CDS5027 CDS5028 CDS5029 CDS5030 CDS5031 CDS5032 CDS5033 CDS5034 CDS5035 CDS5036 CDS5037 CDS5038 CDS5039 CDS5040 CDS5041 CDS5042 CDS5043 CDS5044 CEV3X0076 CEV3X0077 CEV3X0078 CEV3X0079 CEV3X0080 CEV3X0081 CEV3X0082 CEV3X0083 CEV3X0084 CEV3X0085 CEV3X0086 CEV3X0087 CEV3X0088 CEV3X0089 CEV3X0090 CEV3X0091 CEV3X0092 CEV3X0093 CEV3X0094 CEV3X0095 CEV3X0096 CEV3X0097 CEV3X0098 CEV3X0099 CEV3X0100 CEV3X0101 CEV3X0102 CEV3X0103 CEV3X0104 CEV3X0105 CEV3X0106 CEV3X0107 CEV3X0108 CEV3X0109 CEV3X0110 CEV3X0111 CEV3X0112 CEV3X0113 CEV3X0114 CEV3X0115 CEV3X0116 CEV3X0117 CEV3X0118 CEV3X0119 CEV3X0120 CEV3X0121 CEV3X0122 CEV3X0123 CEV3X0124 CEV3X0125 CEV3X0176

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2995-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.